Taiwan FDA registration e89354737c7a540c48e766da04c394db
"Biose" titanium dioxide hernia repair net
TW: “百歐瑟”二氧化鈦疝氣修補網
Taiwan·Risk Class 2·BIOCER ENTWICKLUNGS-GMBH·Registered Nov 06, 2012 – Nov 06, 2027ActiveRegistration details
- Analysis ID
- e89354737c7a540c48e766da04c394db
- Customs Code
- DHA00602408003
Company information
- Manufacturer
- BIOCER ENTWICKLUNGS-GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- HEALTH RIVER INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.3300 Surgical mesh
- Import Information
- import
Dates and status
- Registration Date
- Nov 06, 2012
- Expiry Date
- Nov 06, 2027
About this record
Access comprehensive regulatory information for "Biose" titanium dioxide hernia repair net in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e89354737c7a540c48e766da04c394db 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