"Wacoal" in vitro prosthesis (unsterilized)
Taiwan·Risk Class 1·TRULIFE·Registered Nov 27, 2012 – Nov 27, 2022Cancelled- Analysis ID
- 016f63eb1f565e0cb1540b7ab4636707
- Customs Code
- DHA04401241907
- Manufacturer
- TRULIFE
- Manufacturer Country
- Ireland
- Authorized Representative
- TAIWAN WACOAL CO., LTD.
- 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
- Registration Date
- Nov 27, 2012
- Expiry Date
- Nov 27, 2022
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "Wacoal" 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 016f63eb1f565e0cb1540b7ab4636707 and manufactured by TRULIFE. The authorized representative in Taiwan is TAIWAN WACOAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including WACOAL CORP., TRULIFE, and 2 recent registrations in the same category. 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.