BISICO Provi Temp K

BISICO Bielefelder Dentalsilicone GmbH & Co. KG

Revision date : 2016-07-15

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

General Information

Revision date

2016-07-15

Product name

BISICO Provi Temp K

1.2.1 Relevant identified uses

Temporary material for crowns and bridges

1.2.2. Uses advised against

No further relevant information available

supplier name

Sebastian Zimmermann

Emergency telephone

BISICO Bielefelder Dentalsilicone GmbH & Co. KG

Icons in SDS

Company Information

company name

BISICO Bielefelder Dentalsilicone GmbH & Co. KG

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

info@Bisico.de

GHS Information

Signal word

Warning

Hazard Codes

Hazard statements (CLP)

H315, H317, H319, H335

Hazard statements

Code

Statements

H315

Causes skin irritation

Section 2

2.1 Classification of the substance or mixture

2.1.1. Regulation 1272/2008 Skin Irrit. 2, H315 Causes skin irritation (CLP) and following amendments and Eye Irrit. 2, H319 Causes serious eye irritation adjustments: Skin Sens. 1; H317 May cause allergic skin reaction STOT SE 3; H335 May cause respiratory irritation 2.1.2. 67/548/EEC and The product has to be labeled due to calculation procedure for the 1999/45/EC Directives and “General Classification guideline for preparations of the EU” in the following amendments and latest version. adjustments:

2.2 Label elements

Hazard labelling pursuant to EC Regulation 1272/2008 (CLP) and subsequent amendments and supplements:

Hazard statements

H315 Causes skin irritation H319 Causes serious eye irritation H317 May cause allergic skin reaction H335 May cause respiratory 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. P302+P352 IF ON SKIN: Wash with plenty of soap and water Labeling according to EU guidelines: 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.

PBT Substances

not applicable

vPvB Substances

not applicable

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