neodisher Septo DN

Land: Storbritannien

Sprog: engelsk

Kilde: DrWeigert

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Hent Indlægsseddel (PIL)
22-09-2017
Hent Produktets egenskaber (SPC)
22-09-2017

Tilgængelig fra:

Dr. Weigert

Indlægsseddel

                                Date revised: 31.05.2017
Print date: 31.05.17
3 / GB- 800340-001-03
Version: 3 / GB
Replaces Version: 2 /
GB
SAFETY DATA SHEET IN ACCORDANCE WITH REGULATION (EC) NO
1907/2006 NEODISHER SEPTO DN
Page 1(10)
SECTION 1: IDENTIFICATION OF THE SUBSTANCE/MIXTURE AND OF THE
COMPANY/UNDERTAKING
1.1. PRODUCT IDENTIFIER
neodisher Septo DN
1.2. RELEVANT IDENTIFIED USES OF THE SUBSTANCE OR MIXTURE AND USES
ADVISED AGAINST
USE OF THE SUBSTANCE/PREPARATION
disinfectants
1.3. DETAILS OF THE SUPPLIER OF THE SAFETY DATA SHEET
ADDRESS:
Chemische Fabrik Dr. Weigert GmbH & Co. KG
Mühlenhagen 85
D-20539 Hamburg
Telephone no.
+49 40 789 60 0
Fax no.
+49 40 789 60 120
www.drweigert.com
E-MAIL ADDRESS OF PERSON RESPONSIBLE FOR THIS SDS:
sida@drweigert.de
1.4. EMERGENCY TELEPHONE NUMBER
GBK/ Infotrac: (USA domestic) 1 800 535 5053 or international +1 352
323 3500
SECTION 2: HAZARDS IDENTIFICATION
2.1. CLASSIFICATION OF THE SUBSTANCE OR MIXTURE
CLASSIFICATION (REGULATION (EC) NO. 1272/2008)
Classification (Regulation (EC) No. 1272/2008)
Acute Tox. 4
H302
Acute Tox. 4
H332
Skin Corr. 1B
H314
Eye Dam. 1
H318
Resp. Sens. 1
H334
Skin Sens. 1
H317
STOT SE 3
H335
Aquatic Chronic 3
H412
2.2. LABEL ELEMENTS
LABELLING ACCORDING TO REGULATION (EC) NO 1272/2008
HAZARD PICTOGRAMS
SIGNAL WORD
Danger
HAZARD STATEMENTS
H302+H332
Harmful if swallowed or if inhaled.
H314
Causes severe skin burns and eye damage.
Date revised: 31.05.2017
Print date: 31.05.17
3 / GB- 800340-001-03
Version: 3 / GB
Replaces Version: 2 /
GB
SAFETY DATA SHEET IN ACCORDANCE WITH REGULATION (EC) NO
1907/2006 NEODISHER SEPTO DN
Page 2(10)
H317
May cause an allergic skin reaction.
H334
May cause allergy or asthma symptoms or breathing difficulties if
inhaled.
H412
Harmful to aquatic life with long lasting effects.
EUH071
Corrosive to the respiratory tract.
PRECAUTIONARY STATEMENTS
P260
Do not breathe dust/fume/gas/mist/vapours/spray.
P273
Avoid release to the environment.
P280
Wear protective gloves/protective clothing/eye protection/face
protection.
P303+P361+P353
IF ON SKIN (or ha
                                
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Produktets egenskaber

                                WWW.DRWEIGERT.COM
neodisher
®
Septo DN
Disinfectant for the
automated reprocessing
of flexible endoscopes and
thermolabile instruments
Liquid concentrate
Fields of application:
•
High-level disinfection of flexible endoscopes
and thermolabile instruments in washer
disinfectors
Performance Spectrum:
•
Bactericidal, fungicidal, mycobactericidal and
virucidal activity. Confirmed by certification
•
In the cleaning step the detergent
neodisher MediClean forte is recommended
•
The automated reprocessing process with
neodisher MediClean forte and neodisher Septo
DN fulfils the requirements of DIN EN ISO 15883-
4 with regard to a germ reduction of > 9 log 10 in
the total process.
Special Properties:
•
Very low odour
•
High material compatibility. Suitable for the
endoscopes of all leading manufacturers
•
Free of formaldehyde and quaternary
ammonium compounds
•
The disinfecting activity has been tested and
confirmed according to EN 14885. neodisher
Septo DN conforms to the requirements on
disinfectants for the disinfection of flexible
endoscopes according to DIN EN ISO 15883-4
Application and dosage:
neodisher Septo DN is used in washer disinfectors.
neodisher Septo DN is dosed via the machine’s
integrated dosing device at the beginning of the
disinfecting step. The following parameters must be
observed to achieve the activity spectrum
mentioned below:
bactericidal, fungicidal,
mycobactericidal
and virucidal activity
10 ml/l (1.0 %),
55 °C, 5 min
General instructions on use:
•
For professional use only.
•
The neodisher Septo DN working solution has to
be rinsed off completely with water (preferably
deionised water).
•
Rinse out dosing system including suction hose
with water before changing product.
•
Reprocessing should comply with all ordinances
pursuant to the Medical Device Directive and
should be performed with appropriate validated
processes.
•
Please observe the instrument manufacturer’s
recommendations for reprocessing according to
the requirements of DIN EN ISO 17664.
•
The instr
                                
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