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“Biodermis” Silicone Sheeting(Non-sterile) - Taiwan Registration 4c68bfd17c57184413cb7091fa79bdd1

Access comprehensive regulatory information for “Biodermis” Silicone Sheeting(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 4c68bfd17c57184413cb7091fa79bdd1 and manufactured by BIODERMIS. The authorized representative in Taiwan is GENEJET BIOTECH CO., LTD..

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4c68bfd17c57184413cb7091fa79bdd1
Registration Details
Taiwan FDA Registration: 4c68bfd17c57184413cb7091fa79bdd1
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Device Details

“Biodermis” Silicone Sheeting(Non-sterile)
TW: “百德絲” 疤痕護理矽膠貼片(未滅菌)
Risk Class 1
MD

Registration Details

4c68bfd17c57184413cb7091fa79bdd1

Ministry of Health Medical Device Import No. 014249

DHA09401424901

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 16, 2014

Jun 16, 2024