"Lacrivera" External aesthetic restoration prosthesis (Non-Sterile)
Taiwan·Risk Class 1·MD·LACRIVERA INC.·Registered Oct 01, 2021 – Oct 31, 2023Expired- Analysis ID
- 017c8bbd00c309225f960fed3eb9130f
- License Form
- Ministry of Health Medical Device Import Registration No. 017341
- Customs Code
- DHA08401734105
- Manufacturer
- LACRIVERA INC.
- Manufacturer Country
- United States
- Authorized Representative
- Kangcheng Biomedical Technology 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 and plastic surgical devices
- Product Type (Level 2)
- I3800 In vitro cosmetic repair supplement
- Import Information
- Imported from abroad
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2023
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Access comprehensive regulatory information for "Lacrivera" 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 017c8bbd00c309225f960fed3eb9130f and manufactured by LACRIVERA INC.. The authorized representative in Taiwan is Kangcheng Biomedical Technology Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LACRIVERA 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.