"Lacrivera" External aesthetic restoration prosthesis (Non-Sterile)
Taiwan·Risk Class 1·MD·LACRIVERA INC.·Registered Dec 27, 2016 – Dec 27, 2021Cancelled- Analysis ID
- f725e5278777510125ef1f1f19fed177
- License Form
- Ministry of Health Medical Device Import No. 017341
- Customs Code
- DHA09401734101
- Manufacturer
- LACRIVERA INC.
- Manufacturer Country
- United States
- Authorized Representative
- Kangcheng Biomedical Technology Co., Ltd
- 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
- Dec 27, 2016
- Expiry Date
- Dec 27, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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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 f725e5278777510125ef1f1f19fed177 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.