Taiwan FDA registration 4c68bfd17c57184413cb7091fa79bdd1
“Biodermis” Silicone Sheeting(Non-sterile)
TW: “百德絲” 疤痕護理矽膠貼片(未滅菌)
Taiwan·Risk Class 1·MD·BIODERMIS·Registered Jun 16, 2014 – Jun 16, 2024ExpiredRegistration details
- Analysis ID
- 4c68bfd17c57184413cb7091fa79bdd1
- License Form
- Ministry of Health Medical Device Import No. 014249
- Customs Code
- DHA09401424901
Company information
- Manufacturer
- BIODERMIS
- Manufacturer Country
- United States
- Authorized Representative
- GENEJET BIOTECH CO., LTD.
Product details
- Intended Use
- Limited to the first-level recognition range of the Measures for the Administration of Medical Devices "Scar Treatment Silicone Products (I.4025)".
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4025 Scar Treatment Silicone Products
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 16, 2014
- Expiry Date
- Jun 16, 2024
About this record
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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