Zelgan+

DENTSPLY DeTrey GmbH

Revision date : 2017-04-19

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

Note: Ingredients listed on restricted chemical lists

EC/CAS

14464-46-1

Name of the chemical

Cristobalit (s. u. TRGS 906)

Concentration

N/A

EC/CAS

238-455-4

Name of the chemical

Cristobalit (s. u. TRGS 906)

Concentration

N/A

General Information

Revision date

2017-04-19

Product name

Zelgan+

1.2.1 Relevant identified uses

Dental impression material

1.2.2. Uses advised against

No further relevant information available

Emergency telephone

+49-(0)7531-583-0 8 00 - 17 00 (GMT + 1 00

Icons in SDS

Company Information

company name

DENTSPLY DeTrey GmbH

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

KonstanzDEU.info-sdb@dentsplysirona.com

GHS Information

Signal word

Warning

Hazard Codes

Hazard statements (CLP)

H373

Hazard statements

Code

Statements

H373

May cause damage to organs through prolonged or repeated exposure

Section 2

CLP CLASSIFICATION

STOT RE 2 H373 May cause damage to the lung through prolonged or repeated exposure. Route of exposure: Inhalation.

2.2 Label elements

Labelling according to Regulation (EC) No 1272/2008 The product is classified and labelled according to the CLP regulation.

Hazard pictograms

GHS08

Hazardous Ingredients

cristobalite

Hazard statements

H373 May cause damage to the lung through prolonged or repeated exposure. Route of exposure: Inhalation.

Precautionary statements

P260 Do not breathe dust/fume/gas/mist/vapours/spray. P314 Get medical advice/attention if you feel unwell. P501 Dispose of contents/container in accordance with local/regional/national/international regulations.

Additional information

As this product is a medical device in the meaning of Directive 93/42/EEC and intended for use by the end consumer and is applied in an invasive manner or body contact, it is exempt from the labelling requirements according to regulation 1272/2008. Classification of the mixture is based on the results of an in-vitro test conducted in accordance with guidelines provides by OECD (OECD Test Guidline 437 resp. EU method B.47 - Bovine Corneal Opacity and Permeability (BCOP) Test Method) and GLP certified. For more information refer to section 11.

PBT Substances

Not applicable

vPvB Substances

Not applicable *

SDS Library

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Labels – Generate Secondary Container Labels with just one click.