Note: Ingredients listed on restricted chemical lists
EC/CAS
272-697-1/68909-20-6
Name of the chemical
Silanamine, 1,1,1-trimethyl-N-(trimethylsilyl)-, hydrolysis products with silica
Concentration
10-<30
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
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
1272/2008 Classification of the substance or mixture GB CLP Regulation This mixture is not classified as hazardous in accordance with GB CLP Regulation 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. 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 according
Supplemental label elements
There is no requirement for the product to be specially labelled according to EC directives or the corresponding national laws.
2.3 Other hazards
Due to the physical form (paste) a classification with H373 is not indicated. Inhalation is not possible. The fillers are not bioavailable and accordingly these substances are not considered in the classification of this product
2.1 Classification of the substance or mixture
GB CLP Regulation This mixture is not classified as hazardous in accordance with GB CLP Regulation. *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. 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 according to the Article 31 and Annex II of Regulation (EC) No 1907/2006 (REACH Regulation). This product is classified as a medical device. Medical devices are exempt from the labelling provisions. 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.
