Vectobac 12 AS

Primær information

  • Handelsnavn:
  • Vectobac 12 AS Flydende middel
  • INN (International Name):
  • H14
  • Lægemiddelform:
  • Flydende middel
  • Sammensætning:
  • 1200 ITU/mg Bacilus thuringiensis var. H14
  • Brugt til:
  • Planter
  • Medicin typen:
  • agrokemiske

Dokumenter

  • for den brede offentlighed:
  • Oplysningerne indlægssedlen for dette produkt er i øjeblikket ikke tilgængelig, kan du sende en anmodning til vores kundeservice, og vi vil give dig besked, så snart vi er i stand til at opnå det.


    Anmode informationsbrochure for offentligheden.

Lokation

  • Fås i:
  • Vectobac 12 AS Flydende middel
    Danmark
  • Sprog:
  • dansk

Andre oplysninger

Status

  • Kilde:
  • SEGES Landbrug & Fødevarer
  • Autorisation status:
  • Udgået
  • Autorisationsnummer:
  • Ingen afstandskrav.
  • Sidste ændring:
  • 23-07-2018

Produktresumé

LEVERANDØRBRUGSANVISNING

(Sikkerhedsdatablad)

Udarbejdet efter Arbejdsministeriets bekendtgørelse nr 485 af 16. juni 1995 om stoffer og materialer, § 16, stk. 2.

VECTOBAC

12AS

1. Produktidentifikation

VECTOBAC

12AS

Produkttype:

Biologisk insektmiddel til bekæmpelse

af larver på planter

Leverandør:

Cillus A/S

Tlf.: 4491 6055

Kobbervej 8

Fax.: 4491 6575

2730

Herlev

Kontaktperson: E. Rubæk

2. Oplysning om indholdsstoffer:

Analyse:

VECTOBAC

12AS indeholder 1200

International Toxic Units pr. mg

(1,25%) af Bacillus thuringiensis H-14.

Resten inaktive fyldstoffer (98,75%).

3. Faredeklaration

For mennesker: Undgå kontakt med huden og øjnene.

4. Førstehjælp

Øjne:

Kommer stoffet i øjnene, skylles straks

med vand og læge kontaktes.

Hud:

Forurenet tøj fjernes straks, og forure-

net hud vaskes straks med vand og

sæbe.

Indånding:

Søg frisk luft og hvile

Indtagelse:

Skyl munden, drik rigeligt vand og søg

læge.

Forbrænding:

Ikke brændbart.

5. Forholdsregler ved brand

Produktet bør så vidt muligt fjernes fra brandstedet.

Sluk med pulver, skum eller vandtåge. Hold emballa-

gerne afkølet ved oversprøjtning med vand, hvis udsat

for stærk varme. Undgå indånding af røg og gasser, der

udvikles ved branden.

6. Forholdsregler ved spild

Må ikke hældes i afløb, vandløb eller på jorden.

Evt. spild opsamles med væskeabsorberende materiale,

og dette skal sammen med tom emballage og rester af-

leveres til den kommunale modtageordning.

7. Håndtering og opbevaring

Undgå spild. Brug ansigtsskærm eller beskyttelsesbril-

ler, handsker og forklæde ved udsprøjtning.

S2 -Opbevares utilgængeligt for børn.

S13 -Må ikke opbevares sammen med fødevarer, drik-

kevarer og foderstoffer.

8. Eksponeringskontrol/Personlige værnemidler

Undgå indånding af sprøjtetågen

Undgå kontakt med huden

Brug beskyttelseshandsker. Flerlagshandsker bør fore-

trækkes. Tilsmudset tøj skiftes straks.

Vask huden efter arbejdet.

Efter sprøjtning skal planterne være tørre på bladene,

inden håndtering påbegyndes.

Følg i øvrigt Arbejdstilsynets vejledning og regler om

arbejdstøj og personlige værnemidler.

9. Fysisk-kemiske egenskaber

Tilstandsform:

Vandig suspension

Farve:

Lysebrun

Lugt:

Fermenteringsagtig

Kogepunkt:

Frysepunkt:

Flammepunkt:

ikke brændbart

Opløselighed

i vand:

Opslemning

Vægtfylde:

1,05

ca. 5

10. Stabilitet og reaktivitet

Produktet er lagerfast i mindst 2 år i uåbnet emballage.

Undgå store temperaturudsving. Undgå direkte sollys.

11. Toksikologiske oplysninger

Akut LD-50:

Ved indtagelse > 5000 mg/kg

Ved hudkontakt > 5000 mg/kg

Akut LC-50:

Ved inhalering >5,34 mg/l

Indånding:

Kan give svag irritation.

Hudkontakt:

Kan give svag irritation ved langvarig

påvirkning.

Øjnene:

Stænk i øjnene giver svag irritation

(sviden)

VECTOBAC

12AS

29.04.04

Side 2 af 2

12. Miljøoplysninger

Såvel B.t. som fyldstofferne anses for ikke særlig ska-

delig for miljøet. Se i øvrigt punkt 6.

13. Bortskaffelse

Tom emballage må ikke genanvendes til andet formål.

Tom emballage og rester afleveres til den kommunale

modtageordning.

Rengjort emballage afleveres som dagrenovation.

14. Transportoplysninger

VECTOBAC

12AS er ikke underlagt ADR, hvorfor

der ikke er specielle regler for tranport.

15. Forholdsregler ved brug:

Opbevaring:

VECTOBAC

12AS opbevares frost-

frit.

Må ikke stå i direkte sollys.

Holdbar i uåbnet emballage i mindst 2

år.

Emballagen omrystes grundigt inden det afmålte

kvantum hældes i sprøjtebeholderen under moderat

omrøring.

Tømt og skyllet emballage bortskaffes med dagre-

novationen.

Kommer væsken i øjnene, skyl da omgående med

rigeligt vand

Undgå indånding af sprøjtevæsken.

Anvend ansigtsskærm, handsker og forklæde ved

udsprøjtning.

Planterne skal være tørre inden håndtering påbe-

gyndes.

Vask sprøjteudstyret straks efter arbejdets ophør.

Der kræves ingen særlig uddannelse, dog må unge

under 18 år ikke arbejde med produktet.

16. Brugsanvisning

VECTOBAC

12AS er et biologisk bekæmpelses-

middel, der anvendes mod larver af sørgemyg

(svampemyg) i væksthuse, samt filterfluer (møg-

fluer) i rensningsanlæg og stankelbenlarver på

græsarealer.

"

VECTOBAC

12AS anvendes erhvervsmæssigt

eller privat efter behov.

"

Der er ingen behandlingsfrist. Vask hænder og ud-

styr efter endt udsprøjtning.

"

VECTOBAC

12AS sprøjtevandes på borde, i

potter og på jorden under bordene. Der vandes så

de øverste 3-4 cm af voksemediet er gennemvædet

-ca 2 ltr. væske pr m

. Gennemvanding bør have

fundet sted, inden sprøjtevanding -ikke omvendt.

"

VECTOBAC

12AS optages af sørgemyggens

larver i jorden. Efter 1-2 dages forløb standser lar-

verne fødeoptagelsen og dør.

"

Doseringen er 0,125 - 0,25% styrke i 2 ltr. vand pr.

. Svarende til, at der anvendes 2½ - 5 ml

VECTOBAC

12AS pr m

. 1 ltr. VECTOBAC

12AS rækker således til 200 - 400 m

behandlet

areal.

"

Første behandling umiddelbart efter oppotning.

Behandlingen gentages med 5 - 7 dages interval, i

alt 3 gange. Brug gule limplader til at kontrollere

om flyvningen er holdt op. VECTOBAC

12AS

kan sprøjtevandes sammen med nematoder.

"

VECTOBAC

12AS må ikke blandes med gød-

ning eller lign., der kan neutralisere virkningen -

hverken ved tankblanding eller drypvanding.

Tålsomhed:

Mange plantearter har været prøvet

uden skade, når doseringen overholdes.

Når der skiftes fra en art/sort til en an-

den, eller kulturbetingelserne ændres,

anbefales det at prøve få planter, inden

et helt parti behandles.

VECTOBAC

12AS er anerkendt af

Danmarks Jordbrugsforskning til be-

handling mod larver af sørgemyg på

prydplanter i væksthus med 5 ml pr m

2

Larver af mosestankelben på græsarealer kan være et

problem. Især hvis der året efter skal sås andre afgrø-

der. En total bekæmpelse af mosestankelben er ikke

mulig, men en væsentlig reduktion af larvebestanden

kan forventes.

Tidspunkt:

I oktober måned vælges en mild og fugtig dag. Sprøjt

sidst på dagen når larverne kommer op til overfladen

for at æde af planterne.

Dosering:

2 -2½ ltr. VECTOBAC

12AS pr. ha i mindst 400 ltr.

vand, gerne mere. Evt. i let regnvejr.

Genbehandling:

Hvis klækning af larver sker over en lang periode, kan

behandlingen gentages - evt. næste forår, fortsat med

stor fugtighed i jordoverfladen og gerne i let regn.

Læs mere om bekæmpelse af mosestankelben i ”Mar-

kens sygdomme og skadedyr”.

Udarbejdet af E. Rubæk den 29.04.2004

  • Oplysningerne indlægssedlen for dette produkt er i øjeblikket ikke tilgængelig, kan du sende en anmodning til vores kundeservice, og vi vil give dig besked, så snart vi er i stand til at opnå det.

    Anmode informationsbrochure for offentligheden.



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Memantine Mylan (Mylan S.A.S.)

Memantine Mylan (Mylan S.A.S.)

Memantine Mylan (Active substance: Memantine) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)5972 of Wed, 19 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2660/T/12

Europe -DG Health and Food Safety

14-9-2018

Agenda:  Agenda - CAT agenda of the 12-14 September 2018 meeting

Agenda: Agenda - CAT agenda of the 12-14 September 2018 meeting

Europe - EMA - European Medicines Agency

12-9-2018

The FDA site visit proposal solicitation period for the 2018 Experiential Learning Program is currently OPEN through Wednesday, September 26th 2018 12 pm EST. Click the link to find more about the program & to submit your application  https://go.usa.gov/x

The FDA site visit proposal solicitation period for the 2018 Experiential Learning Program is currently OPEN through Wednesday, September 26th 2018 12 pm EST. Click the link to find more about the program & to submit your application https://go.usa.gov/x

The FDA site visit proposal solicitation period for the 2018 Experiential Learning Program is currently OPEN through Wednesday, September 26th 2018 12 pm EST. Click the link to find more about the program & to submit your application https://go.usa.gov/xPrum  #FDA #MedicalDevice pic.twitter.com/Kyo5z44Os4

FDA - U.S. Food and Drug Administration

12-9-2018

ADCETRIS (Takeda Pharma A/S)

ADCETRIS (Takeda Pharma A/S)

ADCETRIS (Active substance: Brentuximab vedotin) - Centralised - Annual renewal - Commission Decision (2018)5973 of Wed, 12 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2455/R/58

Europe -DG Health and Food Safety

11-9-2018

 Focus group meeting  on dose optimisation of established veterinary antibiotics in the context of summary of product characteristics harmonisation, European Medicines Agency, London, UK, From: 12-Oct-2018, To: 12-Oct-2018

Focus group meeting on dose optimisation of established veterinary antibiotics in the context of summary of product characteristics harmonisation, European Medicines Agency, London, UK, From: 12-Oct-2018, To: 12-Oct-2018

This meeting will allow a direct exchange of views between the Agency’s working party and stakeholders on its draft reflection paper on dose optimisation of established veterinary antibiotics in the context of summary of product characteristics (SPC) harmonisation (EMA/CVMP/849775/2017). It complements the public consultation on this reflection paper ending on 31 January 2019. The reflection paper follows considerations in the report on a pilot project that aimed to develop and test non-experimental appr...

Europe - EMA - European Medicines Agency

5-9-2018

The FDA's site visit proposal solicitation period for the 2018 Experiential Learning Program is currently OPEN through Wednesday, September 26th 2018 at 12 pm EST. Click the link to find more about the program and to submit your application:  https://go.u

The FDA's site visit proposal solicitation period for the 2018 Experiential Learning Program is currently OPEN through Wednesday, September 26th 2018 at 12 pm EST. Click the link to find more about the program and to submit your application: https://go.u

The FDA's site visit proposal solicitation period for the 2018 Experiential Learning Program is currently OPEN through Wednesday, September 26th 2018 at 12 pm EST. Click the link to find more about the program and to submit your application: https://go.usa.gov/xPcpn  #MedicalDevice

FDA - U.S. Food and Drug Administration

7-8-2018

ACMD meeting statement, Meeting 40, 12 April 2018

ACMD meeting statement, Meeting 40, 12 April 2018

Advisory Committee on Medical Devices meeting statement

Therapeutic Goods Administration - Australia

27-7-2018

EU/3/12/1097 (Celgene Europe B.V.)

EU/3/12/1097 (Celgene Europe B.V.)

EU/3/12/1097 (Active substance: Lenalidomide) - Transfer of orphan designation - Commission Decision (2018)5043 of Fri, 27 Jul 2018 European Medicines Agency (EMA) procedure number: EMA/OD/158/12/T/01

Europe -DG Health and Food Safety

27-7-2018

EU/3/12/1091 (bluebird bio (Germany) GmbH)

EU/3/12/1091 (bluebird bio (Germany) GmbH)

EU/3/12/1091 (Active substance: Autologous CD34+ haematopoietic stem cells transduced with lentiviral vector encoding the human betaA-T87Q-globin gene) - Transfer of orphan designation - Commission Decision (2018)5032 of Fri, 27 Jul 2018 European Medicines Agency (EMA) procedure number: EMA/OD/146/12/T/01

Europe -DG Health and Food Safety

27-7-2018

EU/3/12/1003 (bluebird bio (Germany) GmbH)

EU/3/12/1003 (bluebird bio (Germany) GmbH)

EU/3/12/1003 (Active substance: Autologous haematopoietic stem cells transduced with lentiviral vector Lenti-D encoding the human ABCD1 cDNA) - Transfer of orphan designation - Commission Decision (2018)5033 of Fri, 27 Jul 2018 European Medicines Agency (EMA) procedure number: EMA/OD/009/12/T/01

Europe -DG Health and Food Safety

27-7-2018

EU/3/13/1127 (Pfizer Europe MA EEIG)

EU/3/13/1127 (Pfizer Europe MA EEIG)

EU/3/13/1127 (Active substance: Inotuzumab ozogamicin) - Transfer of orphan designation - Commission Decision (2018)5046 of Fri, 27 Jul 2018 European Medicines Agency (EMA) procedure number: EMA/OD/194/12/T/01

Europe -DG Health and Food Safety

27-7-2018

EU/3/12/998 (Orchard Therapeutics Ltd)

EU/3/12/998 (Orchard Therapeutics Ltd)

EU/3/12/998 (Active substance: Autologous CD34+ cells transfected with lentiviral vector containing the Wiskott-Aldrich syndrome protein gene) - Transfer of orphan designation - Commission Decision (2018)5062 of Fri, 27 Jul 2018 European Medicines Agency (EMA) procedure number: EMA/OD/014/12/T/02

Europe -DG Health and Food Safety

27-7-2018

EU/3/12/1066 (Pfizer Europe MA EEIG)

EU/3/12/1066 (Pfizer Europe MA EEIG)

EU/3/12/1066 (Active substance: tafamidis) - Transfer of orphan designation - Commission Decision (2018)5066 of Fri, 27 Jul 2018 European Medicines Agency (EMA) procedure number: EMA/OD/115/12/T/01

Europe -DG Health and Food Safety

22-7-2018

On Friday, Bayer said the permanent birth control device Essure would no longer be sold or distributed in the US for commercial reasons after 12/31/18. This came after FDA’s patient safety action in April restricting sale and distribution of the device an

On Friday, Bayer said the permanent birth control device Essure would no longer be sold or distributed in the US for commercial reasons after 12/31/18. This came after FDA’s patient safety action in April restricting sale and distribution of the device an

On Friday, Bayer said the permanent birth control device Essure would no longer be sold or distributed in the US for commercial reasons after 12/31/18. This came after FDA’s patient safety action in April restricting sale and distribution of the device and earlier agency actions

FDA - U.S. Food and Drug Administration

19-7-2018

EU/3/12/1083 (Global Regulatory Limited)

EU/3/12/1083 (Global Regulatory Limited)

EU/3/12/1083 (Active substance: Humanised single chain monoclonal antibody against CD37) - Transfer of orphan designation - Commission Decision (2018)4839 of Thu, 19 Jul 2018 European Medicines Agency (EMA) procedure number: EMA/OD/128/12/T/02

Europe -DG Health and Food Safety