DIGITGOLD ACTIVE

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  • Trgovački naziv:
  • DIGITGOLD ACTIVE
  • Koristi za:
  • Ljudi
  • Vrsta lijekova:
  • Medicinski uređaj

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Lokalizacija

  • Na raspolaganju u:
  • DIGITGOLD ACTIVE
    Hrvatska
  • Jezik:
  • hrvatski

Druge informacije

Status

  • Izvor:
  • Ecolab
  • Broj odobrenja:
  • 114586E
  • Zadnje ažuriranje:
  • 12-03-2018

Sažetak Opisa Svojstava

SIGURNOSNO -TEHNIČKI LIST

sukladno Uredbi (EZ) br.

1907/2006

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Odj. 1. IDENTIFIKACIJA TVARI/PRIPRAVKA I PODACI O PRAVNOJ ILI FIZIČKOJ OSOBI

1.1 Oznaka proizvoda

Ime proizvoda

DIGITgold ACTIVE

Oznaka proizvoda

114586E

Uporaba tvari/pripravka

Biocid

Vrsta tvari

Preparat

Samo za profesionalne korisnike.

Informacije o razrijeđenom

proizvodu

Nema informacija za razrijeđenje

1.2 Važni utvrđeni načini korištenja tvari ili mješavine i načini korištenja koji se ne preporučaju

Identificirane uporabe

Sredstvo za održavanja prostora kućnih ljubimaca. Polu-

automatski proces.

Njega životinja - manulani postupak

Preporučena ograničenja u

svezi s uporabom

Ograničeno za industrijsku i profesionalnu uporabu.

1.3 Detalji isporučitelja sigurnosno-tehničkog lista

Proizvođač

Ecolab d.o.o.

Zavrtnica 17

10 000, Zagreb Hrvatska 01 632 1600

dijana.kovacic@ecolab.com

1.4 Telefon za izvanredna stanja

Telefon za izvanredna stanja

Telefonski broj Centra za

informacije o trovanju

Hrvatska: 1 476-6464, 06 80-201-199

Datum sakupljanja/revizije

04.04.2014

Verzija

Odj. 2. IDENTIFIKACIJA OPASNOSTI

2.1 Klasifikacija tvari ili smjese

Klasifikacija (UREDBI (EZ) br. 1272/2008)

Akutna toksičnost , Klasa 4

H302

Akutna toksičnost , Klasa 4

H332

Izjedanje kože , Klasa 1B

H314

Osjetljivost dišnog sustava , Klasa 1

H334

Osjetljivost kože , Klasa 1

H317

Specifična toksičnost za ciljne organe/sustavna toksičnost -

jednokratna izloženost , Klasa 3, Dišni sustav

H335

Akutna vodena toksičnost , Klasa 1

H400

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Klasifikacija (67/548/EEZ, 1999/45/EZ)

Xn; ŠKODLJIVO

R20/22

C; KOROZIV

N; OPASNO PO OKOLICU

R42/43

Za cjelokupan sadržaj R upozorenja spomenutih u ovom odsjeku, pogledati odsjek 16.

Za puni tekst H-izjava navedenih u ovom odjeljku pogledajte odjeljak 16.

2.2 Elementi oznake

Označivanje naljepnicom (UREDBI (EZ) br. 1272/2008)

Piktogrami rizika

Upozoravajuća riječ

Opasnost

Upozorenja o opasnosti

H302 + H332

Štetno ako se proguta ili udahne.

H314

Izaziva teške opekotine i oštećenje očiju.

H317

Može uzrokovati alergijsku reakciju kože.

H334

Može uzrokovati alergiju ili simptome astme ili

teškoće u disanju ukoliko se udahne.

H335

Može uzrokovati iritaciju dišnog sustava.

H400

Vrlo otrovno za vodeni svijet.

Obavijesti o opasnosti

Sprječavanje:

P273

Izbjegavati ispuštanje u okoliš.

P280

Nosite zaštitne rukavice/ zaštitu za oči/ zaštitu

za lice.

P285

U slučaju nedovoljnog prozračivanja nositi

sredstva za zaštitu dišnog sustava.

Intervencija:

P303 + P361 + P353

U SLUČAJU DA DOĐE NA KOŽU (na

kosu): Odmah uklonite/ skinite svu

kontaminiranu odjeću. Kožu isperite vodom/

pod tušem.

P304 + P341

U SLUČAJU UDISANJA: U slučaju otežanog

disanja premjestiti unesrećenog na svjež zrak,

ostaviti ga da miruje i staviti ga u udoban

položaj za disanje.

P305 + P351 + P338

U SLUČAJU DA UĐE U OČI: Oprezno

ispirati vodom nekoliko minuta. Izvaditi

kontaktne leće, ako postoje i ako se mogu

sigurno izvaditi. Nastaviti s ispiranjem.

P310

Odmah nazovite TOKSIKOLOŠKI CENTAR ili

liječnika.

Opasne tvari koje se moraju navesti na naljepnici:

Benzalkonij klorid

glutaraldehyde

2.3 Ostale opasnosti

SIGURNOSNO -TEHNIČKI LIST

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Nisu poznati.

Odj. 3. SASTAV/INFORMACIJE O SASTOJCIMA

3.2 Smjese

Opasni sastojci

Kemijski naziv

CAS-br.

EZ-br.

Br. REACH

Klasifikacija

(67/548/EEZ)

Klasifikacija

(UREDBI (EZ) br. 1272/2008)

Koncentracija:

Benzalkonij klorid

68424-85-1

270-325-2

Xn; R22

C; R34

Xi; R41

N; R50

Akutna toksičnostKlasa 4;

H302

Izjedanje kožeKlasa 1B; H314

Ozbiljna povreda okaKlasa 1;

H318

Akutna vodena

toksičnostKlasa 1; H400

>= 10 - < 20

glutaraldehyde

111-30-8

203-856-5

01-2119455549-26

C-N-T;

R23/25-R34-

R42/43-R50

Akutna toksičnostKlasa 3;

H331

Akutna toksičnostKlasa 3;

H301

Akutna vodena

toksičnostKlasa 1; H400

Korozivno za metaleKlasa 1;

H290

Ozbiljno oštećenje

oka/iritacija okaKlasa 1; H318

Osjetljivost dišnog

sustavaKlasa 1; H334

Osjetljivost kožeKlasa 1;

H317

Nagrizanje/iritacija kožeKlasa

1B; H314

Specifična toksičnost za ciljne

organe/sustavna toksičnost -

jednokratna izloženostKlasa

3; H335

>= 10 - < 20

sulfati

10043-01-3

233-135-0

Xi; R41

Ozbiljno oštećenje

oka/iritacija okaKlasa 2; H319

>= 3 - < 5

amini (etanolamin)

68439-70-3

270-414-6

Xn-C-N; R22-

R34-R50

Akutna toksičnostKlasa 4;

H302

Akutna vodena

toksičnostKlasa 1; H400

Nagrizanje/iritacija kožeKlasa

1B; H314

>= 0.25 - < 0.5

alkoholi

67-56-1

200-659-6

T+-T-Xi; R39-

R23-R24-

R25-R36-R10

Zapaljive tekućineKlasa 2;

H225

Akutna toksičnostKlasa 3;

H301

Akutna toksičnostKlasa 3;

H331

Akutna toksičnostKlasa 3;

H311

Specifična toksičnost za ciljne

organe/sustavna toksičnost -

jednokratna izloženostKlasa

1; H370

>= 0.1 - < 0.25

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Za cjelokupan sadržaj R upozorenja spomenutih u ovom odsjeku, pogledati odsjek 16.

Za puni tekst H-izjava navedenih u ovom odjeljku pogledajte odjeljak 16.

Odj. 4. MJERE PRVE POMOĆI

4.1 Opis mjera prve pomoći

U slučaju dodira s očima

Odmah početi ispirati s puno vode, također ispod očnih kapaka, u

trajanju od najmanje 15 minuta. Ukloniti kontaktne leće ukoliko ih

nosite i ako se one lako uklanjaju. Nastaviti ispiranje. Odmah

pozovite liječnika.

U slučaju dodira s kožom

Odmah ispirati s mnogo vode u trajanju od barem 15 minuta. Ako

je moguće, upotrijebiti blag sapun. Operite kontaminiranu odjeću

prije ponovne rabe. Prije ponovne uporabe, temeljito očistiti

obuću. Odmah pozovite liječnika.

U slučaju gutanja

Isprati usta vodom. NE izazivajte povraćanje. Nikada ne davati

bilo što u usta nesvjesnoj osobi. Odmah pozovite liječnika.

U slučaju inhalacije

Premjestiti na svjež zrak. Liječiti simptomatski. Pođite liječniku.

4.2 Najvažniji simptomi i učinci, akutni i odgođeni

Vidjeti odjeljak 11 za detaljnije informacije o utjecajima na zdravlje i mogućim simptomima.

4.3 Oznaka za hitnu medicinsku pomoć i nužan poseban tretman

Liječenje

Liječiti simptomatski.

Odj. 5. MJERE GAŠENJA POŽARA

5.1 Sredstva za gašenje požara

Prikladna sredstva za

gašenje

Upotrijebiti mjere suzbijanja požara koje odgovaraju lokalnim

okolnostima i okolnom ambijentu.

Neprikladna sredstva za

gašenje požara

Nisu poznati.

5.2 Posebne opasnosti koje proizlaze iz tvari ili mješavine

Posebne opasnosti tijekom

suzbijanja požara

Nije zapaljivo niti lako zapaljivo.

Opasni proizvodi izgaranja

ugljikovi oksidi

sumporni oksidi

metalni oksidi

5.3 Mjere opreza za vatrogasce

Posebna zaštitna oprema za

vatrogasce

: Koristiti osobnu zaštitnu opremu.

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Dodatni podaci

: Odvojeno sakupiti otpadnu vodu korištenu za gašenje požara. Ne

ispuštati u odvodni sustav. S požarnim ostacima i vodom koja se

koristila za gašenje požara mora se rukovati u skladu s lokalnim

uredbama. U slučaju požara i/ili eksplozije, ne udisati dimove.

Odj. 6. MJERE KOD SLUČAJNOG ISPUŠTANJA

6.1 Osobne mjere opreza, zaštitna oprema i postupci u slučaju nužde

Savjet za osoblje koje ne

intervenira u hitnim

slučajevima

Osigurati odgovarajuću ventilaciju. Držati ljude podalje i nasuprot

vjetru u odnosu na prolivenu tekućinu/pukotinu iz koje curi.

Izbjegavati udisanje, gutanje i dodir s kožom te očima. Ukoliko se

radnici susreću s količinama većim od graničnih vrijednosti

izloženosti, moraju koristiti odgovarajuće provjerene respiratore.

Osigurajte da cišcenje obavlja samo obuceno ljudstvo. Pogledati

mjere zaštite navedene u odsjecima 7 i 8.

Savjet za osoblje koje

intervenira u hitnim

slučajevima

Ako je specijalizirana odjeća potrebna za rješavanje izlijevanja,

treba obratiti pažnju na bilo kakve informacije u Odjeljku 8 o

prikladnim i neprikladnim materijalima.

6.2 Mjerama zaštite okoliša

Mjerama zaštite okoliša

Ne dozvolite dodir s tlom, površinskim ili podzemnim vodama.

6.3 Načini i materijali za zaustavljanje prolijevanja i čišćenje

Metodama čišćenja

Ako je sigurno, zaustaviti istjecanje.Zaustavite i počistite prolivenu

tvar negorivim materijalom koji ima dobru moć upijanja (npr.

pijesak, zemlja, dijatomejska zemlja, vermikulit) te stavite u

spremnik za odlaganje prema lokalnim/nacionalnim uredbama

(pogledati odsjek 13).Isperite tragove vodom.Za velike izljeve

omeđiti proliveni materijal ili pokupiti materijal kako bi se osiguralo

da ne dospije u odvod.

6.4 Referenca na druge dijelove

Vidjeti Odjeljak 1 za konakt za hitne informacije.

Za osobnu zaštitu pogledati odsjek 8.

Vidjeti Odjeljak 13 za dodatne informacije o obradi otpada.

Odj. 7. RUKOVANJE I SKLADIŠTENJE

7.1 Mjere opreza za sigurno postupanje

Savjeti za sigurno rukovanje

Izbjegavajte dodir s kožom i ocima. Nemojte konzumirati. Ne

udisati prašinu/dim/plin/maglu/pare/aerosol. Spriječiti dodir s

očima, kožom ili odjećom. Nakon rukovanja temeljito operite ruke.

Rabiti samo uz odgovarajuću ventilaciju.

Higijenske mjere

Rukovati u skladu s važećom industrijskom higijenom i

sigurnosnom praksom. Skinuti i oprati kontaminiranu odjeću prije

ponovnog korištenja. Nakon rukovanja temeljito oprati lice, ruke i

izloženu kožu. Osigurati odgovarajući prostor za brzo namakanje

ili ispiranje očiju i tijela u slučaju kontakta ili prskanja opasnim

kemikalijama

7.2 Uvjeti za sigurno pohranjivanje, uključujući i nekompatibilnosti

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Uvjeti skladišnih prostora i

spremnika

Čuvati izvan dohvata djece. Čuvati u dobro zatvorenom

spremniku. Pohranjujte u primjerenim obilježenim

imaspremnicima.

Temperatura skladištenja

0 °C do 40 °C

7.3 Posebne krajnje uporabe

Posebna uporaba

Sredstvo za održavanja prostora kućnih ljubimaca. Polu-

automatski proces.

Njega životinja - manulani postupak

Odj. 8. NADZOR NAD IZLOŽENOŠĆU/OSOBNA ZAŠTITA

8.1 Kontrolni parametri

Ograničenja kod profesionalnog izlaganja

CAS-br.

Sastojci

Vrsta vrijednosti

(Oblik

izloženosti)

Kontrolni

parametri

Ažurirati

Temelj

111-30-8

glutaraldehyde

0.05 ppm

0.2 mg/m3

2009-01-30

HR OEL

STEL

0.05 ppm

0.2 mg/m3

2009-01-30

HR OEL

10043-01-

sulfati

2 mg/m3

2009-01-30

HR OEL

67-56-1

alkoholi

200 ppm

260 mg/m3

2009-01-30

HR OEL

8.2 Nadzor izloženosti

Odgovarajući inženjerski mehanizmi

Tehničke mjere

Djelotvoran odvodno ventilacijski sustav. Održavati vrijednosti

koncentracija u zraku unutar normi za granične vrijednosti

izloženosti na radu.

Individualne mjere zaštite

Higijenske mjere

Rukovati u skladu s važećom industrijskom higijenom i

sigurnosnom praksom. Skinuti i oprati kontaminiranu odjeću prije

ponovnog korištenja. Nakon rukovanja temeljito oprati lice, ruke i

izloženu kožu. Osigurati odgovarajući prostor za brzo namakanje

ili ispiranje očiju i tijela u slučaju kontakta ili prskanja opasnim

kemikalijama

Zaštita očiju/lica (EN 166)

Zaštitne naočale

Stitnik za lice

Zaštita ruku (EN 374)

Nosite sljedeću osobnu zaštitnu opremu:

Nitrilna guma

Butilna guma

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Nepropusne rukavice

U slučaju bilo kakvih znakova razgradnje rukavica ili kemijskog

prodiranja kroz rukavice treba ih ukloniti i zamijeniti novim.

Zaštita kože i tijela (EN

14605)

Osobna zaštitna oprema sastoji se od: odgovarajućih zaštitnih

rukavica, sigurnosnih naočala i zaštitne odjeće

Zaštita organa za disanje

(EN 143, 14387)

Ukoliko se radnici susreću s količinama većim od graničnih

vrijednosti izloženosti, moraju koristiti odgovarajuće provjerene

respiratore.

Nadzor nad zaštitom okoliša

Opći savjeti

: Osigurajte okolicu mjesta pohrane.

Odj. 9. FIZIKALNA I KEMIJSKA SVOJSTVA

9.1 Informacije o osnovnim fizičkim i kemijskim svojstvima

Opće informacije

: tekućina

Boja

: svijetlo plav

Miris

: Sredstva za dezinfekciju

2.7 - 3.1, 100 %

Plamište

Nije primjenjivo

Prag osjetljivosti mirisa

nema raspoloživih podataka

Točka topljenja/Točka

topljenja

nema raspoloživih podataka

Početna točka vrenja i

raspon vrenja

nema raspoloživih podataka

Hlapivost

nema raspoloživih podataka

Zapaljivost (kruta tvar, plin)

nema raspoloživih podataka

Gornja granica

eksplozivnosti

nema raspoloživih podataka

Donja granica eksplozivnosti

nema raspoloživih podataka

Tlak pare

nema raspoloživih podataka

Relativna gustoća pare

nema raspoloživih podataka

Relativna gustoća

1.04 - 1.06

Topljivost u vodi

topivo

Topivost u drugim

sredstvima za otapanje

nema raspoloživih podataka

Koeficijent raspodjele n-

oktanol/voda

nema raspoloživih podataka

Temperatura

samozapaljenja

nema raspoloživih podataka

Termička razgradnja

nema raspoloživih podataka

Viskoznost, kinematička

nema raspoloživih podataka

Eksplozivna svojstva

nema raspoloživih podataka

Oksidirajuća svojstva

Tvar ili mješavina nije klasificirana kao oksidirajuća.

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9.2 Ostali podaci

nema raspoloživih podataka

Odj. 10. STABILNOST I REAKTIVNOST

10.1 Reaktivnost

Nisu poznate opasne reakcije u uvjetima uobičajene uporabe.

10.2 Kemijska stabilnost

Stabilno u normalnim uvjetima.

10.3 Mogućnost opasnih reakcija

Nisu poznate opasne reakcije u uvjetima uobičajene uporabe.

10.4 Uvjeti koje treba izbjegavati

Nisu poznati.

10.5 Nepodudarni materijali

Nisu poznati.

10.6 Opasni proizvodi raspada

ugljikovi oksidi

sumporni oksidi

metalni oksidi

Odj. 11. TOKSIKOLOŠKE INFORMACIJE

11.1 Informacije o toksikološkim posljedicama

Informacije o vjerojatnim

načinima izlaganja

Inhalacija, Dodir s očima, Dodir s kožom

Toksičnost

Akutna oralna toksičnost

: Procjena akutne toksičnosti : 729.57 mg/kg

Akutna toksičnost pri

udisanju

: 4 h Procjena akutne toksičnosti : 12.76 mg/l

Akutna kožna toksičnost

: Procjena akutne toksičnosti : > 2,000 mg/kg

Nagrizanje/iritacija kože

: Nema raspoloživih podataka o ovom proizvodu.

Ozbiljno oštećenje

oka/iritacija oka

: Nema raspoloživih podataka o ovom proizvodu.

Senzibilizacija kože ili dišnih

puteva

: Nema raspoloživih podataka o ovom proizvodu.

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Kancerogenost

: Nema raspoloživih podataka o ovom proizvodu.

Učinci na razmnožavanje

: Nema raspoloživih podataka o ovom proizvodu.

Mutagenost zametnih stanica

: Nema raspoloživih podataka o ovom proizvodu.

Teratogenost

: Nema raspoloživih podataka o ovom proizvodu.

Specifična toksičnost za

ciljne organe/sustavna

toksičnost (jednokratna

izloženost)

: Nema raspoloživih podataka o ovom proizvodu.

Specifična toksičnost za

ciljne organe/sustavna

toksičnost (opetovana

izloženost)

: Nema raspoloživih podataka o ovom proizvodu.

Aspiracijska toksičnost

: Nema raspoloživih podataka o ovom proizvodu.

Sastojci

Akutna oralna toksičnost

: Benzalkonij klorid

LD50 štakor: 344 mg/kg

glutaraldehyde

LD50 štakor: 150 mg/kg

Akutna toksičnost pri

udisanju

: glutaraldehyde

4 h LC50 štakor: 3 mg/l

4 h LC50 štakor: > 0.5 mg/l

sulfati

4 h LC50 štakor: > 1 mg/l

Akutna kožna toksičnost

: Benzalkonij klorid

LD50 zec: 3,340 mg/kg

glutaraldehyde

LD50 štakor: 1,503 mg/kg

sulfati

LD50 zec: 5,000 mg/kg

Potencijalno djelovanje na zdravlje

Oči

Uzrokuje ozbiljno oštećenje očiju.

Koža

Prouzrokuje teške opekline kože. Može prouzrokovati alergijsku

reakciju kože.

Gutanje

Prouzrokuje opekline probavnog trakta.

Štetno ako se proguta.

Inhalacija

Štetno ukoliko se udahne. Može uzrokovati alergiju ili simptome

astme ili teškoće u disanju ukoliko se udahne. Može uzrokovati

iritaciju dišnog sustava. Može prouzrokovati nadraživanje nosa,

grla i pluća.

SIGURNOSNO -TEHNIČKI LIST

sukladno Uredbi (EZ) br. 1907/2006

DIGITgold ACTIVE

114586E

10 / 13

Kronično izlaganje

Zdravstvena oštećenja nisu poznata, niti su za očekivati pri

normalnoj upotrebi.

Iskustvo s izlaganjem ljudi

Dodir s očima

Crvenilo, Bol, Nagrizanje

Dodir s kožom

Crvenilo, Bol, Nadraživanje, Nagrizanje, alergijska reakcija

Gutanje

Nagrizanje, Bolovi u trbuhu

Inhalacija

Nadraženost dišnih puteva, Kašalj, Može uzrokovati alergiju ili

simptome astme ili teškoće u disanju ukoliko se udahne.

Odj. 12. EKOLOŠKE INFORMACIJE

12.1 Ekotoksičnost

Utjecaj na okoliš

Vrlo otrovno za vodeni svijet.

Proizvod

Otrovnost za ribe

: nema raspoloživih podataka

Toksično za daphnia i ostale

vodene beskičmenjake.

: nema raspoloživih podataka

Otrovnost za alge

: nema raspoloživih podataka

Sastojci

Otrovnost za ribe

: Benzalkonij klorid

96 h LC50 ribe : 0.515 mg/l

sulfati

96 h LC50 ribe : 22.8 mg/l

alkoholi

96 h LC50: 15,400 mg/l

Sastojci

Toksično za daphnia i ostale

vodene beskičmenjake.

: glutaraldehyde

48 h EC50 Daphnia: 0.35 mg/l

12.2 Postojanost i razgradivost

nema raspoloživih podataka

12.3 Bioakumulacijski potencijal

nema raspoloživih podataka

12.4 Mobilnost u zemlji

nema raspoloživih podataka

12.5 Rezultati procjene PBT i vPvB svojstava

Proizvod

SIGURNOSNO -TEHNIČKI LIST

sukladno Uredbi (EZ) br. 1907/2006

DIGITgold ACTIVE

114586E

11 / 13

Ocjena

Ova tvar/smjesa ne sadrži komponente koje se smatraju

postojanim, bioakumulirajućima i toksičnima (PBT), ili jako

postojanim i jako bioakumulirajućima (VPvB) na razinama od

0,1% ili više.

12.6 Ostali štetni učinci

nema raspoloživih podataka

Odj. 13. ZBRINJAVANJE

Odlažite u skladu s europskim direktivama o otpadu i opasnom otpadu.Kodove otpada bi trebao

odrediti korisnik, po mogućnosti u dogovoru s nadležnim organima za zbrinjavanje otpada.

13.1 Metode upravljanja otpadom

Proizvod

: Proizvod ne smije ući u odvodne kanale, izvore vode ili tlo. Uvijek

kada je moguće se preferira recikliranje od odlaganja ili

spaljivanja. Ukoliko se ne može sprovesti recikliranje, odlagati u

skladu s lokalnim uredbama. Otpad odlažite na ovlaštena

odlagališta namijenjena toj svrsi.

Kontaminirana ambalaža

: Odlagati kao neupotrijebljen proizvod. Prazne spremnike treba

dostaviti ovlaštenoj osobi za postupanje s otpadom na recikliranje

ili odlaganje. Prazni spremnici se ne smiju ponovno upotrebljavati.

Europski katalog otpada

: 200114* - kiseline

Odj. 14. INFORMACIJE O PRIJEVOZU

Pošiljatelj je odgovoran osigurati da pakiranje, etiketiranje i obilježavanje je u skladu sa odabranim

načinom prijevoza.

Kopneni prijevoz (ADR/ADN/RID)

14.1 UN broj

1903

14.2 Točan naziv pošiljke

UN-a

SREDSTVO ZA DEZINFEKCIJU, TEKUĆE, KOROZIVNO, N.D.N.

(Benzalkonij klorid, glutaraldehyde)

14.3 Klasa(e) opasnosti

prijevoza

14.4 Skupinu pakiranja

14.5 Opasnosti za okoliš

14.6 Posebne mjere opreza

za korisnike

Nijedan

Zračni prijevoz (IATA)

14.1 UN broj

1903

14.2 Točan naziv pošiljke

UN-a

Disinfectant, liquid, corrosive, n.o.s.

(Benzalkonij klorid, glutaraldehyde)

14.3 Klasa(e) opasnosti

prijevoza

14.4 Skupinu pakiranja

14.5 Opasnosti za okoliš

14.6 Posebne mjere opreza

za korisnike

Nijedan

SIGURNOSNO -TEHNIČKI LIST

sukladno Uredbi (EZ) br. 1907/2006

DIGITgold ACTIVE

114586E

12 / 13

Morski prijevoz (IMDG/IMO)

14.1 UN broj

1903

14.2 Točan naziv pošiljke

UN-a

DISINFECTANT, LIQUID, CORROSIVE, N.O.S.

(Benzalkonij klorid, glutaraldehyde)

14.3 Klasa(e) opasnosti

prijevoza

14.4 Skupinu pakiranja

14.5 Opasnosti za okoliš

14.6 Posebne mjere opreza

za korisnike

Nijedan

14.7 Prijevoz u rasutom

stanju prema aneksu II

konvencije MARPOL 73/78 i

IBC kodu

Nije primjenjivo

Odj. 15. INFORMACIJE O PROPISIMA

15.1 Uredbe/propisi koji se odnose na sigurnost, zdravlje i okoliš, a koji su specifični za tvar ili

mješavinu

Tuzemna odredba

Obratiti pažnju na Direktivu 94/33/EZ o zaštiti mladih ljudi na poslu.

Druge uredbe

Zakon o kemikalijama, Pravilnik o razvrstavanju, označavanju,

obilježavanju i pakiranju opasnih kemikalija-rađen prema DSD i

DPD direktivama, Pravilnik o razvrstavanju, označavanju,

obilježavanju i pakiranju opasnih kemikalija-rađen prema CLP-u

Zako

15.2 Procjena sigurnosti kemikalija

Ovaj proizvod sadrži supstance za koje su Procjene sigurnosti kemikalija još uvijek neophodne.

Odj. 16. OSTALE INFORMACIJE

Cjelovit tekst R-fraza

Zapaljivo.

Škodljivo ako se proguta.

Otrovno ako se udahne.

R23/25

Otrovno za udisanje i gutanje.

Otrovno za dodir s kožom.

Otrovno ako se proguta.

Uzrokuje opekline.

Nadražuje oci.

Opasnost od ozbiljnih neizljecivih posljedica.

Rizik od ozbiljnog oštecenja oka.

R42/43

Može izazvati osjetljivost ako se udahne i dode u dodir s kožom.

Jako otrovno za vodene organizme.

Cjelovit tekst H-izjava

H225

Lako zapaljiva tekućina i para

H290

Može biti korozivno za metale.

H301

Otrovno ukoliko se proguta.

H302

Štetno ako se proguta.

SIGURNOSNO -TEHNIČKI LIST

sukladno Uredbi (EZ) br. 1907/2006

DIGITgold ACTIVE

114586E

13 / 13

H311

Otrovno u dodiru s kožom.

H314

Izaziva teške opekotine i oštećenje očiju.

H317

Može uzrokovati alergijsku reakciju kože.

H318

Uzrokuje ozbiljno oštećenje očiju.

H319

Uzrokuje ozbiljnu iritaciju očiju.

H331

Otrovno ukoliko se udahne.

H334

Može uzrokovati alergiju ili simptome astme ili teškoće u disanju ukoliko

se udahne.

H335

Može uzrokovati iritaciju dišnog sustava.

H370

Uzrokuje oštećenje organa.

H400

Vrlo otrovno za vodeni svijet.

Cjelovit tekst ostalih skraćenica

Pripremio

Regulatory Affairs

Brojevi navedeni u sigurnosnim listama (MSDS) dani su u obliku: 1,000 ,000 = 1 miljun and 1,000

= 1 tisuća. 0.1 = 1 destinka i 0.001 = 1 tisucinka.

PREPRAVLJENI PODACI: Znatne promjene zdravstvenih podataka za ovu reviziju su obilježene

na lijevoj margini MSDS-a.

Podaci u ovom sigurnosno-tehničkom listu odgovaraju našim saznanjima, informacijama i

uvjerenjima na dan izdavanja istog. Informacije sadržane u njemu, dane su samo kao smjernice

za sigurno rukovanje, upotrebu, postupanje, skladištenje, prijevoz i odlaganje otpada i nisu

garancija ili specifikacija kvalitete. Podaci se odnose isključivo na navedenu tvar/smjesu i nisu

nužno važeći za istu tu tvar/smjesu ukoliko se ista koristi sa bilo kojim drugim tvarima ili u bilo

kojem drugom postupku koji nije specificiran u tekstu.

  • Informativni letak za ovaj proizvod trenutno nije dostupan, možete poslati zahtjev na našu službu za korisnike, a mi ćemo vas obavijestiti čim smo u mogućnosti da ga dobiju.

    Zatražite informativni letak za javnost.



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Europe -DG Health and Food Safety

16-11-2018

Latuda (Aziende Chimiche Riunite Angelini Francesco - A.C.R.A.F. S.p.A.)

Latuda (Aziende Chimiche Riunite Angelini Francesco - A.C.R.A.F. S.p.A.)

Latuda (Active substance: lurasidone) - Centralised - Renewal - Commission Decision (2018)7674 of Fri, 16 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2713/R/20

Europe -DG Health and Food Safety

16-11-2018

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Europe -DG Health and Food Safety

15-11-2018

Flixabi (Samsung Bioepis NL B.V.)

Flixabi (Samsung Bioepis NL B.V.)

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15-11-2018

alitretinoin

alitretinoin

alitretinoin (Active substance: alitretinoin) - Centralised - Art 28 - (PSUR - Commission Decision (2018)7675 of Thu, 15 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/PSUSA/90/201801

Europe -DG Health and Food Safety

14-11-2018

Jinarc (Otsuka Pharmaceutical Netherlands B.V.)

Jinarc (Otsuka Pharmaceutical Netherlands B.V.)

Jinarc (Active substance: tolvaptan) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)7604 of Wed, 14 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2788/T/20

Europe -DG Health and Food Safety

14-11-2018

Clopidogrel ratiopharm (Teva B.V.)

Clopidogrel ratiopharm (Teva B.V.)

Clopidogrel ratiopharm (Active substance: clopidogrel) - Centralised - Yearly update - Commission Decision (2018)7602 of Wed, 14 Nov 2018

Europe -DG Health and Food Safety

14-11-2018

Desloratadine ratiopharm (ratiopharm GmbH)

Desloratadine ratiopharm (ratiopharm GmbH)

Desloratadine ratiopharm (Active substance: desloratadine) - Centralised - Yearly update - Commission Decision (2018)7603 of Wed, 14 Nov 2018

Europe -DG Health and Food Safety

14-11-2018

Ebymect (AstraZeneca AB)

Ebymect (AstraZeneca AB)

Ebymect (Active substance: dapagliflozin / metformin) - Centralised - 2-Monthly update - Commission Decision (2018)7605 of Wed, 14 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4162/WS/1380

Europe -DG Health and Food Safety

14-11-2018

Laventair Ellipta (Glaxo Group Ltd)

Laventair Ellipta (Glaxo Group Ltd)

Laventair Ellipta (Active substance: umeclidinium bromide / vilanterol trifenatate) - Centralised - Yearly update - Commission Decision (2018)7611 of Wed, 14 Nov 2018

Europe -DG Health and Food Safety

13-11-2018

EU/3/17/1863 (Celgene Europe B.V.)

EU/3/17/1863 (Celgene Europe B.V.)

EU/3/17/1863 (Active substance: Autologous T lymphocyte-enriched population of cells transduced with a lentiviral vector encoding a chimeric antigen receptor targeting human B cell maturation antigen with 4-1BB and CD3-zeta intracellular signalling domains) - Transfer of orphan designation - Commission Decision (2018)7574 of Tue, 13 Nov 2018 European Medicines Agency (EMA) procedure number: EMA/OD/270/16/02

Europe -DG Health and Food Safety

13-11-2018

EU/3/17/1836 (Zogenix GmbH)

EU/3/17/1836 (Zogenix GmbH)

EU/3/17/1836 (Active substance: Fenfluramine hydrochloride) - Transfer of orphan designation - Commission Decision (2018)7576 of Tue, 13 Nov 2018 European Medicines Agency (EMA) procedure number: EMA/OD/233/16/T/01

Europe -DG Health and Food Safety

13-11-2018

EU/3/13/1219 (Zogenix GmbH)

EU/3/13/1219 (Zogenix GmbH)

EU/3/13/1219 (Active substance: Fenfluramine hydrochloride) - Transfer of orphan designation - Commission Decision (2018)7575 of Tue, 13 Nov 2018 European Medicines Agency (EMA) procedure number: EMA/OD/140/13/T/01

Europe -DG Health and Food Safety

13-11-2018

EU/3/17/1964 (Incyte Biosciences Distribution B.V.)

EU/3/17/1964 (Incyte Biosciences Distribution B.V.)

EU/3/17/1964 (Active substance: Itacitinib) - Transfer of orphan designation - Commission Decision (2018)7573 of Tue, 13 Nov 2018 European Medicines Agency (EMA) procedure number: EMA/OD/169/17/T/01

Europe -DG Health and Food Safety

12-11-2018

Efavirenz/Emtricitabine/Tenofovir disoproxil Zentiva (Zentiva, k.s.)

Efavirenz/Emtricitabine/Tenofovir disoproxil Zentiva (Zentiva, k.s.)

Efavirenz/Emtricitabine/Tenofovir disoproxil Zentiva (Active substance: efavirenz / emtricitabine / tenofovir disoproxil) - Centralised - Yearly update - Commission Decision (2018)7547 of Mon, 12 Nov 2018

Europe -DG Health and Food Safety

12-11-2018

Ruconest (Pharming Group N.V.)

Ruconest (Pharming Group N.V.)

Ruconest (Active substance: Conestat alfa) - Centralised - Yearly update - Commission Decision (2018)7548 of Mon, 12 Nov 2018

Europe -DG Health and Food Safety

12-11-2018

Spinraza (Biogen Netherlands B.V.)

Spinraza (Biogen Netherlands B.V.)

Spinraza (Active substance: nusinersen) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)7550 of Mon, 12 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4312/T/10

Europe -DG Health and Food Safety

6-11-2018

Symkevi (Vertex Pharmaceuticals (Europe) Limited)

Symkevi (Vertex Pharmaceuticals (Europe) Limited)

Symkevi (Active substance: tezacaftor/ivacaftor) - Centralised - Authorisation - Commission Decision (2018)7415 of Tue, 06 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4682

Europe -DG Health and Food Safety

6-11-2018

Trelegy Ellipta (GlaxoSmithKline Trading Services Limited)

Trelegy Ellipta (GlaxoSmithKline Trading Services Limited)

Trelegy Ellipta (Active substance: fluticasone furoate/umeclidinium/vilanterol) - Centralised - 2-Monthly update - Commission Decision (2018)7416 of Tue, 06 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4363/WS/1369

Europe -DG Health and Food Safety

6-11-2018

Elebrato Ellipta (GlaxoSmithKline Trading Services Limited)

Elebrato Ellipta (GlaxoSmithKline Trading Services Limited)

Elebrato Ellipta (Active substance: fluticasone furoate/umeclidinium/vilanterol) - Centralised - 2-Monthly update - Commission Decision (2018)7417 of Tue, 06 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4781/WS/1369

Europe -DG Health and Food Safety

6-11-2018

Neulasta (Amgen Europe B.V.)

Neulasta (Amgen Europe B.V.)

Neulasta (Active substance: Pegfilgrastim) - Centralised - Yearly update - Commission Decision (2018)7420 of Tue, 06 Nov 2018

Europe -DG Health and Food Safety

6-11-2018

Samsca (Otsuka Pharmaceutical Netherlands B.V.)

Samsca (Otsuka Pharmaceutical Netherlands B.V.)

Samsca (Active substance: tolvaptan) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)7419 of Tue, 06 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/980/T/36

Europe -DG Health and Food Safety

5-11-2018

EU/3/18/2070 (Accelsiors CRO and Consultancy Services Ltd)

EU/3/18/2070 (Accelsiors CRO and Consultancy Services Ltd)

EU/3/18/2070 (Active substance: (6aR,10aR)-3-(1,1-dimethylheptyl)-delta8-tetrahydro-cannabinol-9-carboxylic acid) - Orphan designation - Commission Decision (2018)7271 of Mon, 05 Nov 2018 European Medicines Agency (EMA) procedure number: EMA/OD/114/18

Europe -DG Health and Food Safety

5-11-2018

Improvac (Zoetis Belgium S.A.)

Improvac (Zoetis Belgium S.A.)

Improvac (Active substance: Not available) - Centralised - Yearly update - Commission Decision (2018)7381 of Mon, 05 Nov 2018

Europe -DG Health and Food Safety

1-11-2018

Zolvix (Elanco GmbH)

Zolvix (Elanco GmbH)

Zolvix (Active substance: monepantel) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)7383 of Thu, 01 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/V/C/000154/T/0024

Europe -DG Health and Food Safety

1-11-2018

Protopic (Leo Pharma A/S)

Protopic (Leo Pharma A/S)

Protopic (Active substance: Tacrolimus) - Centralised - Yearly update - Commission Decision (2018)7343 of Thu, 01 Nov 2018

Europe -DG Health and Food Safety

1-11-2018

Dexdomitor (Orion Corporation)

Dexdomitor (Orion Corporation)

Dexdomitor (Active substance: dexmedetomidine hydrochloride) - Centralised - Yearly update - Commission Decision (2018)7380 of Thu, 01 Nov 2018

Europe -DG Health and Food Safety

1-11-2018

Taxespira (Hospira UK Limited)

Taxespira (Hospira UK Limited)

Taxespira (Active substance: docetaxel) - Centralised - Withdrawal - Commission Decision (2018)7368 of Thu, 01 Nov 2018

Europe -DG Health and Food Safety

31-10-2018

Integrilin (GlaxoSmithKline (Ireland) Limited)

Integrilin (GlaxoSmithKline (Ireland) Limited)

Integrilin (Active substance: Eptifibatide) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)7340 of Wed, 31 Oct 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/230/T/79

Europe -DG Health and Food Safety

31-10-2018

Volibris (GlaxoSmithKline (Ireland) Limited)

Volibris (GlaxoSmithKline (Ireland) Limited)

Volibris (Active substance: Ambrisentan) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)7339 of Wed, 31 Oct 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/839/T/56

Europe -DG Health and Food Safety

31-10-2018

AMGEVITA (Amgen Europe B.V.)

AMGEVITA (Amgen Europe B.V.)

AMGEVITA (Active substance: adalimumab) - Centralised - Yearly update - Commission Decision (2018)7341 of Wed, 31 Oct 2018

Europe -DG Health and Food Safety

31-10-2018

Imraldi (Samsung Bioepis NL B.V.)

Imraldi (Samsung Bioepis NL B.V.)

Imraldi (Active substance: adalimumab) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)7344 of Wed, 31 Oct 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4279/T/15

Europe -DG Health and Food Safety

31-10-2018

Evista (Daiichi Sankyo Europe GmbH)

Evista (Daiichi Sankyo Europe GmbH)

Evista (Active substance: Raloxifene hydrochloride) - Centralised - Yearly update - Commission Decision (2018)7342 of Wed, 31 Oct 2018

Europe -DG Health and Food Safety

31-10-2018

Eporatio (ratiopharm GmbH)

Eporatio (ratiopharm GmbH)

Eporatio (Active substance: epoetin theta) - Centralised - Yearly update - Commission Decision (2018)7336 of Wed, 31 Oct 2018

Europe -DG Health and Food Safety

31-10-2018

Viramune (Boehringer Ingelheim International GmbH)

Viramune (Boehringer Ingelheim International GmbH)

Viramune (Active substance: nevirapine) - Centralised - Yearly update - Commission Decision (2018)7337 of Wed, 31 Oct 2018

Europe -DG Health and Food Safety

30-10-2018

EU/3/14/1250 (Akcea Therapeutics UK Ltd)

EU/3/14/1250 (Akcea Therapeutics UK Ltd)

EU/3/14/1250 (Active substance: Phosphorothioate oligonucleotide targeted to transthyretin) - Transfer of orphan designation - Commission Decision (2018)7282 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/098/13/T/01

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2080 (Freeline Therapeutics Ltd)

EU/3/18/2080 (Freeline Therapeutics Ltd)

EU/3/18/2080 (Active substance: Recombinant adeno-associated viral vector serotype S3 containing codon-optimised expression cassette encoding human coagulation factor IX variant) - Orphan designation - Commission Decision (2018)7281 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/127/18

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2079 (Spark Therapeutics Ireland Ltd)

EU/3/18/2079 (Spark Therapeutics Ireland Ltd)

EU/3/18/2079 (Active substance: Recombinant adeno-associated viral vector containing a bioengineered capsid and a codon-optimised expression cassette to drive the expression of the SQ form of a B-domain deleted human coagulation factor VIII) - Orphan designation - Commission Decision (2018)7280 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/104/18

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2078 (Sellas Life Sciences Limited)

EU/3/18/2078 (Sellas Life Sciences Limited)

EU/3/18/2078 (Active substance: Peptides YMFPNAPYL, SGQAYMFPNAPYLPSCLES, RSDELVRHHNMHQRNMTKL and PGCNKRYFKLSHLQMHSRKHTG) - Orphan designation - Commission Decision (2018)7279 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/091/18

Europe -DG Health and Food Safety