Taiwan FDA registration 8f05c385f44be9334092d1bf9f1084fa
TiO2Mesh Light Surgical mesh implant
TW: “百歐瑟”輕量型二氧化鈦疝氣修補網
Taiwan·Risk Class 2·MD·BIOCER ENTWICKLUNGS-GMBH·Registered Nov 09, 2022 – Nov 09, 2027ActiveRegistration details
- Analysis ID
- 8f05c385f44be9334092d1bf9f1084fa
- License Form
- Ministry of Health Medical Device Import No. 036036
- Customs Code
- DHA05603603609
Company information
- Manufacturer
- BIOCER ENTWICKLUNGS-GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- HEALTH RIVER INC.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I3300 Surgical mesh
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 09, 2022
- Expiry Date
- Nov 09, 2027
About this record
Access comprehensive regulatory information for TiO2Mesh Light Surgical mesh implant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8f05c385f44be9334092d1bf9f1084fa and manufactured by BIOCER ENTWICKLUNGS-GMBH. The authorized representative in Taiwan is HEALTH RIVER INC..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices