Taiwan FDA registration 8ead2dc672ba42cb4ea5ae4b3ab78d63
Immunospecific chemiluminescence matrix (unsterilized)
TW: 免疫特化學發光基質(未滅菌)
Taiwan·Risk Class 1·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED·Registered Sep 23, 2009 – Sep 23, 2014CancelledRegistration details
- Analysis ID
- 8ead2dc672ba42cb4ea5ae4b3ab78d63
- Customs Code
- DHA04400814902
Company information
- Manufacturer
- SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- SIEMENS LIMITED
Product details
- Intended Use
- Limited to the first level identification scope of "General Purpose Reaction Reagents (B.4010)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.4010 Reaction Reagents for General Purposes
- Import Information
- import
Dates and status
- Registration Date
- Sep 23, 2009
- Expiry Date
- Sep 23, 2014
- Cancellation Date
- Jul 31, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Immunospecific chemiluminescence matrix (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8ead2dc672ba42cb4ea5ae4b3ab78d63 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED. The authorized representative in Taiwan is SIEMENS LIMITED.
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