3M Impregum Penta Soft Base Paste

3M United Kingdom PLC

Revision date : 2020-05-06

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GHS09 GHS07
Health risk rating 4
Safety risk rating 1
Environmental risk rating 4

Note: Ingredients listed on restricted chemical lists

EC/CAS

272-489-0/68855-54-9

Name of the chemical

diatomaceous earth, soda ash flux-calcined

Concentration

<10

General Information

Version

3.00

Revision date

2020-05-06

Product name

3M Impregum Penta Soft Base Paste

1.2.1 Relevant identified uses

Medical device; refer to Instructions for Use

1.2.2. Uses advised against

For use only by dental professionals

Emergency telephone

+44 (0)1344 858 000

Icons in SDS

GHS07 GHS09

Company Information

company name

3M United Kingdom PLC

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

tox.uk@mmm.com

GHS Information

Signal word

WARNING

Hazard Codes

Hazard statements (CLP)

H317, H319, H400, H411

Hazard statements

Code

Statements

H317

May cause an allergic skin reaction

Section 2

SECTION 2: Hazards identification

Regulation (EC) No. 1272/2008 Classification of the substance or mixture

Signal word

WARNING.

Hazard pictograms

GHS07 (Exclamation mark) |GHS09 (Environment) | Ingredients: Ingredient CAS Nbr EC No. % by Wt Laurylimidazole 4303-67-7 224-314-4 < 1 Mint flavor 68917-18-0 < 0.5 Mint flavor 98561-44-5 308-804-6 < 0.5

Hazard statements

H317 May cause an allergic skin reaction. H400 Very toxic to aquatic life. H411 Toxic to aquatic life with long lasting effects.

Prevention

P280E Wear protective gloves. P273 Avoid release to the environment.

Response

P333 + P313 If skin irritation or rash occurs: Get medical advice/attention.

Disposal

P501 Dispose of contents/container in accordance with applicable local/regional/national/internationa regulations. Notes on labelling H319 not assigned per test data.

2.3 Other hazards

For information on hazards and safe use, please consider the corresponding sections of this document.

2.1 Classification of the substance or mixture

CLP REGULATION (EC) No 1272/2008 This product is a medical device as defined in Directive 93/42/EEC (MDD) respectively Regulation (EU) 2017/745 (MDR), which is invasive or used in direct physical contact with the human body, and therefore is exempt from the requirements of classification and labelling according to Regulation (EC) No. 1272/2008 (CLP; Article 1, paragraph 5). Although not required, the classification and label information, as applicable, is provided below. CLASSIFICATION: Skin Sensitization, Category 1A - Skin Sens. 1A; H317 Hazardous to the Aquatic Environment (Acute), Category 1 - Aquatic Acute 1; H400 Hazardous to the Aquatic Environment (Chronic), Category 2 - Aquatic Chronic 2; H411 For full text of H phrases, see Section 16.

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