neodisher Septo 3000

Land: Verenigd Koninkrijk

Taal: Engels

Bron: DrWeigert

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Bijsluiter Bijsluiter (PIL)
22-09-2017
Productkenmerken Productkenmerken (SPC)
22-09-2017

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Dr. Weigert

Bijsluiter

                                Date revised: 02.02.2016
Print date: 02.02.16
2 / GB- 800882-001-02
Version: 2 / GB
Replaces Version: 1 /
GB
SAFETY DATA SHEET IN ACCORDANCE WITH REGULATION (EC) NO
1907/2006 NEODISHER SEPTO 3000
Page 1(12)
SECTION 1: IDENTIFICATION OF THE SUBSTANCE/MIXTURE AND OF THE
COMPANY/UNDERTAKING
1.1. PRODUCT IDENTIFIER
neodisher Septo 3000
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. 1A
H314
Eye Dam. 1
H318
Skin Sens. 1
H317
Resp. Sens. 1
H334
STOT SE 3
H335
Muta. 2
H341
Carc. 1B
H350
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.
Date revised: 02.02.2016
Print date: 02.02.16
2 / GB- 800882-001-02
Version: 2 / GB
Replaces Version: 1 /
GB
SAFETY DATA SHEET IN ACCORDANCE WITH REGULATION (EC) NO
1907/2006 NEODISHER SEPTO 3000
Page 2(12)
H314
Causes severe skin burns and eye damage.
H317
May cause an allergic skin reaction.
H334
May cause allergy or asthma symptoms or breathing difficulties if
inhaled.
H335
May cause respiratory irritation.
H341
Suspected of causing genetic defects.
H350
May cause cancer.
PRECAUTIONARY STATEMENTS
P201
Obtain special instructions before use.
P260
Do not breathe dust/fume/gas/mist/vapours/spray.
P280
Wear protective gloves/protective clothing/eye protection/face
protection.
P303+P361+
                                
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Productkenmerken

                                WWW.DRWEIGERT.COM
neodisher
®
Septo 3000
With the above information, to our current knowledge we describe our
product regarding safety necessities, but we do not involve any
quality description or promise certain properties.
Chemische Fabrik Dr. Weigert GmbH & Co. KG
Tel.: +49-40-7 89 60-0
info@drweigert. de
Mühlenhagen 85 • D-20539 Hamburg
Fax: +49-40-7 89 60-120
www. drweigert. de
Disinfectant for the manual
reprocessing of thermostable
and thermolabile instruments
Liquid concentrate
Fields of application:
•
Disinfection of thermostable and thermolabile
medical devices in immersion or ultrasonic baths
•
Also suitable for the disinfection of flexible
endoscopes
Performance spectrum:
•
Bactericidal, fungicidal, mycobactericidal,
virucidal and sporicidal activity. Confirmed
by certification
•
Suitable for all standard materials such as
stainless steel, chrome-nickel steel, plastics,
rubber, porcelain and glass
•
For manual pre-cleaning the use of neodisher
MediClean forte is recommended
Special properties:
•
Wide range of activity, even with short
action times
•
Excellent material compatibility
•
VAH
1
-listed
, on the list of the IHO
2
for disinfectants
with virucidal activity
Application and dosage:
neodisher Septo 3000 is used in immersion and
ultrasonic baths. Depending on the desired activity
the working solution must be prepared according to
the below mentioned dosing recommendations. The
working solution must always be prepared with cold
water (at room temperature).
Clean the instruments resp. endoscopes thoroughly,
e.g. with the detergent neodisher MediClean forte
prior to disinfection. Then place the instruments
resp. endoscopes into the neodisher Septo 3000
working solution and adhere to the below
mentioned contact times.
Never exceed the limit for the exposure time in
ultrasonic baths which is recommended by the
instrument manufacturer. For correct disinfection in
ultrasonic baths the contact times must be
observed.
Open and dismantle the instruments as far as
possible. Ensure that a
                                
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