Futurabond U Liquid 1

VOCO GmbH

Revision date : 2025-11-24

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GHS05 GHS07
Health risk rating 4
Safety risk rating 1
Environmental risk rating 1

Note: Ingredients listed on restricted chemical lists

EC/CAS

868-77-9

Name of the chemical

2-hydroxyethyl methacrylate

Concentration

25-50% 5-10%

EC/CAS

72869-86-4

Name of the chemical

11,14-Dioxa-2,9-diazaheptadec-16-enoic Acid, 4,4,6,16-tetramethyl-10,15-dioxo, 2-[(2-methyl-1-oxo-2-propenyl)oxy]ethyl ester (31)

Concentration

5-10%

General Information

Revision date

2025-11-24

Product name

Futurabond U Liquid 1

1.2.1 Relevant identified uses

Bonding

1.2.2. Uses advised against

No further relevant information available

Emergency telephone

+49 (0) 4721 - 719 - 0

Icons in SDS

GHS05 GHS07 M004 M009 M011

Company Information

company name

VOCO GmbH

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

info@voco.de

GHS Information

Signal word

Danger

Hazard Codes

Hazard statements (CLP)

H314, H317, H318

Hazard statements

Code

Statements

H314

Causes severe skin burns and eye damage

Section 2

SECTION 2: Hazards identification

Regulation (EC) No. 1272/2008 Classification of the substance or mixture This product is a medical device in accordance with Directive 93/42/EEC on medical devices or Regulation EU) 2017/745 (MDR), which is used invasively or in contact with the body. It is therefore exempt from the

Hazard pictograms

GHS05 GHS07

Hazard statements

Causes severe skin burns and eye damage. May cause an allergic skin reaction.

Precautionary statements

Avoid breathing dust/fume/gas/mist/vapors/spray Avoid release to the environment. Wear protective gloves / eye protection / face protection. If swallowed: Rinse mouth. Do NOT induce vomiting. If on skin: Wash with plenty of water. IF INHALED: Remove person to fresh air and keep comfortable for breathing. If in eyes: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Dispose of contents/container in accordance with local/regional/national/international regulations.

Other hazards

Use only for intended scope of application

PBT Substances

Not applicable

vPvB Substances

Not applicable

2.1 Classification of the substance or mixture

This product is a medical device in accordance with Directive 93/42/EEC on medical devices or Regulation (EU) 2017/745 (MDR), which is used invasively or in contact with the body. It is therefore exempt from the classification and labelling requirements of Regulations (EC) 1907/2006 (REACH, Art. 2 (6) c)) and (EC) 1272/2008 ((UK) CLP, Article 1 (5) d). The classification criteria of Regulation (EC) No 1272/2008 are not directly applicable to this product, but are considered by us as an orienting basis for assessment.The health and environmental hazards have been assessed and classified on the basis of the information known to us on the components and their reaction processes.The following hazards based on the classification criteria of Regulation (EC) No 1272/2008 for humans and the environment cannot be excluded: GHS05 Corrosion Skin Corrosion 1A H314 Causes severe skin burns and eye damage. Eye Damage 1 H318 Causes serious eye damage. GHS07 Sensitization - Skin 1 H317 May cause an allergic skin reaction. ꞏ Additional information: Health effects are based on the unmixed/uncured material. This product is a medical device within the meaning of the US Federal Food, Drug and Cosmetic Act, the Canadian Medical Devices Regulations (CMDR) SOR/98-282 and the Canadian Food and Drugs Act R.S.S., 1985, c. F-27, which is used invasively or in contact with the body. It is therefore exempt from the classification and labeling requirements of the US Hazard Communication Standard (HCS), WHMIS, the Canadian Hazardous Products Act (HPA) and the Canadian Hazardous Products Regulations Act (HPR). (Contd. on page 2) US (Contd. of page 1)

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