Spiex cytoplasm separator cannula set
Taiwan·Risk Class 2·BIOSAFE Ltd·Registered Oct 30, 2006 – Oct 30, 2026Active- Analysis ID
- 5a25e463fb9e21e4f4a5ecf7fda8a99d
- Customs Code
- DHA00601739205
- 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
- Oct 30, 2006
- Expiry Date
- Oct 30, 2026
Top companies providing products similar to "Spiex cytoplasm separator cannula set"
Recently registered similar products
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 5a25e463fb9e21e4f4a5ecf7fda8a99d 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.