Taiwan FDA registration 392d97c857b59af2979d21121ed9188f
"Antis" in vitro cosmetic repair supplement (unsterilized)
TW: “安緹司”體外美容用修復彌補物(未滅菌)
Registration details
- Analysis ID
- 392d97c857b59af2979d21121ed9188f
- Customs Code
- DHA04400746405
Company information
- Manufacturer
- ANTEIS SA
- Manufacturer Country
- Switzerland
- Authorized Representative
- BEAUTYCOM BIOTECHNOLOGY CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of medical equipment management measures for in vitro cosmetic repair supplements (I.3800).
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.3800 Repair supplement for cosmetic use in the body
- Import Information
- import
Dates and status
- Registration Date
- Feb 11, 2009
- Expiry Date
- Feb 11, 2014
- Cancellation Date
- Jan 09, 2017
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Antis" in vitro cosmetic repair supplement (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 392d97c857b59af2979d21121ed9188f and manufactured by ANTEIS SA. The authorized representative in Taiwan is BEAUTYCOM BIOTECHNOLOGY CO., LTD..
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