Taiwan FDA registration 18d1152ac173bd5f2775d02d5be4ee69
Bierxi Cell cryogenic equipment for in vitro diagnostics
TW: 碧而喜 體外診斷用細胞冷凍設備
Taiwan·Risk Class 1·P&C INTERNATIONAL·Registered Sep 09, 2009 – Sep 09, 2014CancelledRegistration details
- Analysis ID
- 18d1152ac173bd5f2775d02d5be4ee69
- Customs Code
- DHA04400806509
Company information
- Manufacturer
- P&C INTERNATIONAL
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- NEOASIA LTD.
Product details
- Intended Use
- Limited to the first level identification range of cell cryogenic equipment and reactants (B.9225) for in vitro diagnosis of medical device management methods.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9225 Cell freezing equipment and reagents for in vitro diagnostics
- Import Information
- import
Dates and status
- Registration Date
- Sep 09, 2009
- Expiry Date
- Sep 09, 2014
- Cancellation Date
- Aug 14, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Bierxi Cell cryogenic equipment for in vitro diagnostics in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 18d1152ac173bd5f2775d02d5be4ee69 and manufactured by P&C INTERNATIONAL. The authorized representative in Taiwan is NEOASIA LTD..
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