"DETEKT" External Aesthetic Restoration Prosthesis (Non-Sterile)
Taiwan·Risk Class 1·MD·DETEKT TECHNOLOGY INC.·Registered Oct 01, 2021 – Oct 31, 2026Active- Analysis ID
- 439515147e110aab60658bec7ed2dd7e
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 009054
- Manufacturer
- DETEKT TECHNOLOGY INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- DETEKT TECHNOLOGY INC.
- 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 and plastic surgical devices
- Product Type (Level 2)
- I3800 In vitro cosmetic repair supplement
- Import Information
- Produced in Taiwan, China
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
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Access comprehensive regulatory information for "DETEKT" External Aesthetic Restoration Prosthesis (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 439515147e110aab60658bec7ed2dd7e and manufactured by DETEKT TECHNOLOGY INC.. The authorized representative in Taiwan is DETEKT TECHNOLOGY INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DETEKT TECHNOLOGY INC., and 1 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.