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
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)