Note: Ingredients listed on restricted chemical lists
EC/CAS
14464-46-1
Name of the chemical
Cristobalit (s. u. TRGS 906)
Concentration
50-75%
General Information
Version
6
Revision date
2023-03-06
Product name
Memoreg 2 Base
1.2.2. Uses advised against
No further relevant information available
Emergency telephone
+61 (02) 9153 0311
Icons in SDS
Company Information
company name
Kulzer Australia Pty Ltd
GHS Information
Signal word
Danger
Hazard Codes
Hazard statements (CLP)
H372
Hazard statements
Code
Statements
H372
Causes damage to organs through prolonged or repeated exposure
Section 2
SECTION 2: Hazards identification
1272/2008 Classification of the substance or mixture STOT RE 1 H372 Causes damage to the lung through prolonged or repeated exposure. Route of exposure: Inhalation Additional information Since the product is a medical device in the sense of Directive 93/42/EEC (MDD) or the Regulation (EU) 2017/745 (MDR), that is intended for the end user and is used invasively or with physical contact, it is exempted from the classification and labeling obligation according to
2.2 Label elements
The product is classified and labelled according to the Globally Harmonised System (GHS).
Hazard pictograms
GHS08
Signal word
Danger
Hazardous Ingredients
cristobalite
Hazard statements
Causes damage to the lung through prolonged or repeated exposure. Route of exposure: Inhalation.
Precautionary statements
Do not breathe dust. Wash thoroughly after handling. Avoid release to the environment. Wear protective gloves / eye protection. Wear protective clothing. Get medical advice/attention if you feel unwell.
Additional information
see 2.1
2.3 Other hazards
(Contd. on page 2) AU (Contd. of page 1)
PBT Substances
Not applicable
vPvB Substances
Not applicable
2.1 Classification of the substance or mixture
STOT RE 1 H372 Causes damage to the lung through prolonged or repeated exposure. Route of exposure: Inhalation. · Additional information: Since the product is a medical device in the sense of Directive 93/42/EEC (MDD) or the Regulation (EU) 2017/745 (MDR), that is intended for the end user and is used invasively or with physical contact, it is exempted from the classification and labeling obligation according to Regulation (EC) 1272/2008.
