Spiex cytoplasm separator cannula set
Taiwan·Risk Class 2·BIOSAFE Ltd·Registered Dec 27, 2011 – Dec 27, 2026Active- Analysis ID
- dc2ab4c93cac3c77595786e50c5cee6f
- Customs Code
- DHA00602317802
- Manufacturer
- BIOSAFE Ltd
- Manufacturer Country
- Switzerland
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9100 Containers for the collection and disposal of blood and blood components
- Import Information
- import
- Registration Date
- Dec 27, 2011
- Expiry Date
- Dec 27, 2026
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Access comprehensive regulatory information for Spiex cytoplasm separator cannula set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dc2ab4c93cac3c77595786e50c5cee6f and manufactured by BIOSAFE Ltd. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BIOSAFE Ltd, 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.