Ufi Gel hard C base

VOCO GmbH

Revision date : 2025-12-05

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

Note: Ingredients listed on restricted chemical lists

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% ≤1%

General Information

Revision date

2025-12-05

Product name

Ufi Gel hard C base

1.2.1 Relevant identified uses

Luting of prosthetic teeth

1.2.2. Uses advised against

No further relevant information available

Emergency telephone

+49 (0) 4721 - 719 - 0

Icons in SDS

GHS07 M004 M009 M010 M011 T016

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

Warning

Hazard Codes

Hazard statements (CLP)

H317, H320

Hazard statements

Code

Statements

H317

May cause an allergic skin reaction

Section 2

SECTION 2: Hazards identification

Potential health effects

are based on the unmixed/uncured material Under FDA regulations this product is classified as a medical device. Medical devices are exempt from the labelling provisions of GHS according to the Hazard Communication Standard (HCS). 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

GHS07

Hazard statements

Causes eye irritation. May cause an allergic skin reaction.

Precautionary statements

Wear protective gloves. If on skin: Wash with plenty of water. If skin irritation or rash occurs: Get medical advice/attention. Dispose of contents/container in accordance with local/regional/national/international regulations.

2.3 Other hazards

Use only for intended scope of application. None

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: GHS07 Sensitization - Skin 1 H317 May cause an allergic skin reaction. Eye Irritation 2B H320 Causes eye irritation. ꞏ Additional information: Health effects are based on the unmixed/uncured material. (Contd. on page 2) US (Contd. of page 1)

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