Note: Ingredients listed on restricted chemical lists
EC/CAS
201-297-1/80-62-6
Name of the chemical
methacrylic acid, methyl ester
Concentration
2120102014-82 <0.5
EC/CAS
204-881-4/128-37-0
Name of the chemical
2,6-di-tert-butyl-p-cresol
Concentration
<0.5
General Information
Version
2.00
Revision date
2022-12-07
Product name
3M RELYX Unicem Aplicap/Maxicap Liquid
1.2.1 Relevant identified uses
Medical device; refer to Instructions for Use
Emergency telephone
+44 (0)1344 858 000
Icons in SDS
Company Information
company name
3M Ireland Limited
e-mail address of the competent person responsible for the Safety Data Sheet
tox.uk@mmm.com
GHS Information
Signal word
Danger
Hazard Codes
Hazard statements (CLP)
H317, H318, H412
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
Hazard pictograms
GHS05 (Corrosion) |GHS07 (Exclamation mark) | Ingredients: Ingredient CAS Nbr EC No. % by Wt Phosphorylated methacrylate 700-757-3 40 - 50 Triethyleneglycol dimenthacrylate (TEGDMA) 109-16-0 203-652-6 20 - 35 Methyl methacrylate (MMA) 80-62-6 201-297-1 < 0.5
Hazard statements
H318 Causes serious eye damage. H317 May cause an allergic skin reaction. H412 Harmful to aquatic life with long lasting effects.
Prevention
P280B Wear protective gloves and eye/face protection.
Response
P305 + P351 + P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P310 Immediately call a POISON CENTRE or doctor/physician. P333 + P313 If skin irritation or rash occurs: Get medical advice/attention.
2.3 Other hazards
For information on hazards and safe use, please consider the corresponding sections of this document. This material does not contain any substances that are assessed to be a PBT or vPvB
2.1 Classification of the substance or mixture
CLP REGULATION (EC) No 1272/2008 The health and environmental classifications of this material have been derived using the calculation method, except in cases where test data are available or the physical form impacts classification. Classification(s) based on test data or physical form are noted below, if applicable. 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: Serious Eye Damage/Eye Irritation, Category 1 - Eye Dam. 1; H318 Skin Sensitization, Category 1 - Skin Sens. 1; H317 Hazardous to the Aquatic Environment (Chronic), Category 3 - Aquatic Chronic 3; H412 For full text of H phrases, see Section 16.
