Taiwan FDA registration 12a1fe999411cd47104febb0fe1995d6
Sigu Blood Cell Separator
TW: 思沛克血球細胞分離機
Taiwan·Risk Class 3·BIOSAFE Ltd·Registered Oct 26, 2012 – Oct 26, 2027ActiveRegistration details
- Analysis ID
- 12a1fe999411cd47104febb0fe1995d6
- Customs Code
- DHA00602414505
Company information
- Manufacturer
- BIOSAFE Ltd
- Manufacturer Country
- Switzerland
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
Product details
- 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.9245 Automated hemocytoseparator
- Import Information
- import
Dates and status
- Registration Date
- Oct 26, 2012
- Expiry Date
- Oct 26, 2027
About this record
Access comprehensive regulatory information for Sigu Blood Cell Separator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 12a1fe999411cd47104febb0fe1995d6 and manufactured by BIOSAFE Ltd. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices