Taiwan FDA registration 88c5b73602684b220574c95a5301a87d
Syncope immunoglobulin fluorescent binder (unsterilized)
TW: 協克免疫球蛋白螢光結合劑 (未滅菌)
Taiwan·Risk Class 1·EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG·Registered May 21, 2010 – May 21, 2020CancelledRegistration details
- Analysis ID
- 88c5b73602684b220574c95a5301a87d
- Customs Code
- DHA04400884002
Company information
- Manufacturer
- EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG
- Manufacturer Country
- Germany
- Authorized Representative
- SEEKERS BIOMEDICAL CO., LTD.
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
- May 21, 2010
- Expiry Date
- May 21, 2020
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Syncope immunoglobulin fluorescent binder (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 88c5b73602684b220574c95a5301a87d and manufactured by EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG. The authorized representative in Taiwan is SEEKERS BIOMEDICAL CO., LTD..
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