Taiwan FDA registration b86307d514faa9dcecb84b59d90750dd
"Siemens" Immune Assay Diluent (Unsterilized)
TW: "西門子" 免疫特檢體稀釋液 (未滅菌)
Taiwan·Risk Class 1·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED·Registered Jun 14, 2012 – Jun 14, 2017CancelledRegistration details
- Analysis ID
- b86307d514faa9dcecb84b59d90750dd
- Customs Code
- DHA04401182704
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
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jun 14, 2012
- Expiry Date
- Jun 14, 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 "Siemens" Immune Assay Diluent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b86307d514faa9dcecb84b59d90750dd and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED. The authorized representative in Taiwan is SIEMENS LIMITED.
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