“Bimini” Puregraft System
Taiwan·Risk Class 2·MD·Bimini Health Tech·Registered Jul 26, 2023 – Jul 26, 2028Active- Analysis ID
- 0c5cd0331f564ace234e513250770666
- License Form
- Ministry of Health Medical Device Import No. 036680
- Customs Code
- DHA05603668000
- Manufacturer
- Bimini Health Tech
- Manufacturer Country
- United States
- Authorized Representative
- Beleli Biotechnology Co., Ltd
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I5040 Grease Extractor
- Import Information
- Imported from abroad
- Registration Date
- Jul 26, 2023
- Expiry Date
- Jul 26, 2028
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Access comprehensive regulatory information for “Bimini” Puregraft System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0c5cd0331f564ace234e513250770666 and manufactured by Bimini Health Tech. The authorized representative in Taiwan is Beleli Biotechnology Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Bimini Health Tech, 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.