Taiwan FDA registration 6d1972c72edaac2c562b66c81a35429e
"ANDLIFE" AFTAMED Hydrogel Wound Dressing (Non-Sterile)
TW: "安德生醫" 愛敷美水性傷口敷料 (未滅菌)
Taiwan·Risk Class 1·MD·BIOPLAX LIMITED·Registered Jun 15, 2015 – Jun 15, 2025ExpiredRegistration details
- Analysis ID
- 6d1972c72edaac2c562b66c81a35429e
- License Form
- Ministry of Health Medical Device Import No. 015338
- Customs Code
- DHA09401533802
Company information
- Manufacturer
- BIOPLAX LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- ANDLIFE INC.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Waterborne Wound and Burn Covering Materials (I.4022)".
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4022 Waterborne wound and burn coverings
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 15, 2015
- Expiry Date
- Jun 15, 2025
About this record
Access comprehensive regulatory information for "ANDLIFE" AFTAMED Hydrogel Wound Dressing (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 6d1972c72edaac2c562b66c81a35429e and manufactured by BIOPLAX LIMITED. The authorized representative in Taiwan is ANDLIFE INC..
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