Mucopren Soft

Kettenbach GmbH & Co. KG

Revision date : 2026-03-10

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GHS08
Health risk rating 5
Safety risk rating 4
Environmental risk rating 4

Note: Ingredients listed on restricted chemical lists

EC/CAS

68909-20-6

Name of the chemical

Silanamine, 1,1,1-trimethyl-N-(trimethylsilyl)-, hydrolysis products with silica

Concentration

28.75%

Listed in

General Information

Revision date

2026-03-10

Product name

Mucopren Soft

1.2.1 Relevant identified uses

Permanently soft, polyvinyl siloxane liner Medical device for use in dentistry, observe instructions for use

1.2.2. Uses advised against

Use by untrained dental personnel and/or unapproved areas of application

Emergency telephone

49(0) 2774/705-0, +49 (0)2774/705-66

Icons in SDS

M004 M009 M010 P022 GHS08

Company Information

company name

Kettenbach GmbH & Co. KG

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

info@kettenbach.com

GHS Information

Signal word

Warning

Section 2

SECTION 2: Hazards identification

Classification of the chemical

Special rules for supplemental label elements for certain mixtures

99 percent of the mixture consists of ingredient(s) of unknown toxicity (inhalation).

2.3 Other hazards

Due to the physical form (paste) a classification with H373 is not indicated. Inhalation is not possible.

2.1 Classification of the substance or mixture

29 CFR Part 1910.1200 This mixture is not classified as hazardous in accordance with Regulation 29 CFR 1910.1200(d). *Safety Information Sheet for Medical Devices* The particulars given in the Safety Information Sheet only apply to the described product in connection with its appropriate utilization. These particulars are based on the latest state of our knowledge and information. In particular, they serve the purpose of describing our product under the aspect of hazards caused by such product and pertaining safety actions. They do not constitute any guarantee of product quality and/or quality features. The particulars given in this Safety Information Sheet are not required in accordance with 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 (29 CFR § 1910.1200). They merely serve the purpose of providing sufficient information on the voluntary basis with a view to ensure the safe utilization of such substance/mixture/product.

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