Taiwan FDA registration 43e5fc511aba7ef735df435018837e9f
Dermanson Minster C-reactive protein Flax reagent group
TW: 德曼遜敏斯特C反應蛋白弗列克斯試劑組
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Registered Jan 18, 2012 – Jan 18, 2017CancelledRegistration details
- Analysis ID
- 43e5fc511aba7ef735df435018837e9f
- Customs Code
- DHA00602309205
Company information
- Manufacturer
- SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- SIEMENS LIMITED
Product details
- Intended Use
- Quantitatively measure the concentration of C-reactive protein (CRP) in human serum and heparinized plasma with the Dimension Vista system.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.5270 C反應蛋白免疫試驗系統
- Import Information
- import
Dates and status
- Registration Date
- Jan 18, 2012
- Expiry Date
- Jan 18, 2017
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Dermanson Minster C-reactive protein Flax reagent group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 43e5fc511aba7ef735df435018837e9f and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH. The authorized representative in Taiwan is SIEMENS LIMITED.
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