Coltoflax mix

Coltène/Whaledent AG

Revision date : 2015-06-18

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GHS07 GHS08
Health risk rating 4
Safety risk rating 1
Environmental risk rating 3

General Information

Revision date

2015-06-18

Product name

Coltoflax mix

CAS No.

24577-34-2

Icons in SDS

Company Information

company name

Coltène/Whaledent AG

e-mail address of the competent person responsible for the Safety Data Sheet

info.ch@coltene.com

GHS Information

Signal word

Warning

Hazard Codes

Hazard statements (CLP)

H315, H319, H373, H413

Hazard statements

Code

Statements

H315

Causes skin irritation

Section 2

EU Classification

Directive 67/548/EEC or 1999/45/EC

Hazard statements

Xn - Harmful Causes skin irritation. Causes serious eye irritation. May cause damage to organs through prolonged or repeated exposure. May cause long lasting harmful effects to aquatic life. H315 Causes skin irritation. H319 Causes serious eye irritation. H373 May cause damage to organs through prolonged or repeated exposure. H413 May cause long lasting harmful effects to aquatic life.

R-phrase(s)

Harmful: danger of serious damage to health by prolonged exposure if swallowed. May cause long-term adverse effects in the aquatic environment.

Hazard categories

Skin corrosion/irritation: Skin Irrit. 2 Serious eye damage/eye irritation: Eye Irrit. 2 Specific target organ toxicity - repeated exposure: STOT RE 2 Hazardous to the aquatic environment: Aquatic Chronic 4

Hazardous Ingredients

Alkyl silicates

Signal word

Warning

Hazard pictograms

GHS07-GHS08

Precautionary statements

P280 Wear protective gloves/protective clothing/eye protection/face protection. P302+P352 IF ON SKIN: Wash with plenty of water. P332+P313 If skin irritation occurs: Get medical advice/attention. 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. P314 Get medical advice/attention if you feel unwell. P273 Avoid release to the environment.

Supplemental label elements

Medical devices as defined in Directive 93/42/EEC and which are invasive or used in direct physical contact with the human body, are exempted from the provisions of Regulation (EC) No 1272/2008 (CLP/GHS) usually if they are in the finished state and intended for the final user.

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