neodisher Z Dental

Riik: Suurbritannia

keel: inglise

Allikas: DrWeigert

Saadav alates:

Dr. Weigert

Infovoldik

Date revised: 23.08.2017
Print date: 23.08.17
3 / GB- 800155-009-01
Version: 3 / GB
Replaces Version: 2 /
GB
SAFETY DATA SHEET IN ACCORDANCE WITH REGULATION (EC) NO
1907/2006 NEODISHER Z DENTAL
Page 1(8)
SECTION 1: IDENTIFICATION OF THE SUBSTANCE/MIXTURE AND OF THE
COMPANY/UNDERTAKING
1.1. PRODUCT IDENTIFIER
neodisher Z Dental
1.2. RELEVANT IDENTIFIED USES OF THE SUBSTANCE OR MIXTURE AND USES
ADVISED AGAINST
USE OF THE SUBSTANCE/PREPARATION
Washing and cleaning products (including solvent based products)
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.
[phone]
Fax no.
[phone]
www.drweigert.com
E-MAIL ADDRESS OF PERSON RESPONSIBLE FOR THIS SDS:
[e-mail]
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)
Eye Irrit. 2
H319
2.2. LABEL ELEMENTS
LABELLING ACCORDING TO REGULATION (EC) NO 1272/2008
HAZARD PICTOGRAMS
SIGNAL WORD
Warning
HAZARD STATEMENTS
H319
Causes serious eye irritation.
PRECAUTIONARY STATEMENTS
P280
Wear protective gloves/protective clothing/eye protection/face
protection.
P305+P351+P338
IF IN EYES: Rinse cautiously with water for several minutes. Remove
contact
lenses, if present and easy to do. Continue rinsing.
P337+P313
If eye irritation persists: Get medical advice/attention.
Dispose only when container is empty and closed. For disposal of
product
residues, refer to Safety Data Sheet.
Date revised: 23.08.2017
Print date: 23.08.17
3 / GB- 800155-009-01
Version: 3 / GB
Replaces Version: 2 /
GB
SAFETY DATA SHEET IN ACCORDANCE WITH REGULATION (EC) NO
1907/2006 NEODISHER Z DENTAL
Page 2(8)
2.3. OTHER HAZARDS
No special hazards have to be mentioned.
SECTION 3: COMPOSITION/INFORMATION ON INGREDIENTS
3.2. MIXTURES
HAZARDOUS INGREDIENTS
CITRIC ACID

Toote omadused

NEODISHER
® Z DENTAL
Acidic neutralization agent for the automated reprocessing of dental
instruments
liquid concentrate
Chemische Fabrik Dr. Weigert GmbH & Co. KG
Telefon: [phone] - 0
E-Mail: info @drweigert.de
Mühlenhagen 85, D – 20539 Hamburg
Telefax: (040) 789 60 - 120
Internet: www. drweigert.de
Die Angaben dieses Merkblattes beruhen auf unseren derzeitigen
Kenntnissen und Erfahrungen. Sie befreien den
Verwender nicht von eigenen Prüfungen und Versuchen. Eine rechtlich
verbindliche Zusicherung bestimmter
Eigenschaften kann hieraus nicht abgeleitet werden.
With the above information, which is appropriate to our current
knowledge we describe
our product regarding possible safety necessities, but we do not
involve any quality description
or promise certain properties.
Main fields of application:
Neutralisation of alkaline residues when automatically cleaning dental
instruments,
transmission instruments and dental utensils such as trays, cups for
mouth rinsing and
kidney dishes.
Characteristics:
neodisher Z Dental is material compatible. Basically, neodisher Z
Dental should be
used as a neutralizing agent where a particular material compatibility
is necessary. It is
highly recommendable for the reprocessing of transmission instruments,
which must
not be reprocessed with neutralizers containing acidic phosphorous.
neodisher Z Dental is free of surfactants.
Application and dosage:
neodisher Z Dental is used in washer disinfectors for dental
instruments. The dosage is
1- 2 ml/l.
Use suitable devices for dosing neodisher Z.
For avoiding water stains the use of deionised water in the final
rinse is recommended.
At the same time anodized aluminium is protected.
The neodisher Z Dental solution has to be rinsed off completely with
water (preferably
with deionised water).
Do not mix with other products. Rinse out dosing system including hose
with water before
changing product.
Reprocessing should comply with all ordinances pursuant to the Medical
Device Directive
and should be performed with appropriate validat