Taiwan FDA registration fba1328ebd42f16e21da2625ecacca17
"Chu Laifu" in vitro prosthesis (unsterilized)
TW: “初萊富”體外用義乳（未滅菌）
Taiwan·Risk Class 1·TRULIFE·Registered Sep 20, 2010 – Sep 20, 2015CancelledRegistration details
- Analysis ID
- fba1328ebd42f16e21da2625ecacca17
- Customs Code
- DHA04400920902
Company information
- Manufacturer
- TRULIFE
- Manufacturer Country
- Ireland
- Authorized Representative
- JE CHEENG INDUSTRAL 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
- Sep 20, 2010
- Expiry Date
- Sep 20, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Chu Laifu" in vitro prosthesis (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fba1328ebd42f16e21da2625ecacca17 and manufactured by TRULIFE. The authorized representative in Taiwan is JE CHEENG INDUSTRAL 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