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“Biodermis” Silicone Gel (Non-sterile) - Taiwan Registration 97a721669ecb9580e53c6e0e5c04233e

Access comprehensive regulatory information for “Biodermis” Silicone Gel (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 97a721669ecb9580e53c6e0e5c04233e and manufactured by BIODERMIS. The authorized representative in Taiwan is GENEJET BIOTECH CO., LTD..

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97a721669ecb9580e53c6e0e5c04233e
Registration Details
Taiwan FDA Registration: 97a721669ecb9580e53c6e0e5c04233e
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Device Details

“Biodermis” Silicone Gel (Non-sterile)
TW: “百德絲”疤痕護理凝膠(未滅菌)
Risk Class 1
MD

Registration Details

97a721669ecb9580e53c6e0e5c04233e

Ministry of Health Medical Device Import No. 014225

DHA09401422500

Company Information

United States

Product Details

Limited to the first-level recognition range of the Measures for the Administration of Medical Devices "Scar Treatment Silicone Products (I.4025)".

I General and plastic surgical devices

I4025 Scar Treatment Silicone Products

Imported from abroad

Dates and Status

Jun 06, 2014

Jun 06, 2024