Taiwan FDA registration 04705a707e02a0af3c7e2595b57ab0b6
Nanobia D-binary reagent
TW: 納諾比亞D-二元體試劑
Taiwan·Risk Class 2·SEKISUI MEDICAL CO., LTD. TSUKUBA PLANT·Registered May 03, 2013 – May 03, 2018CancelledRegistration details
- Analysis ID
- 04705a707e02a0af3c7e2595b57ab0b6
- Customs Code
- DHA00602468205
Company information
- Manufacturer
- SEKISUI MEDICAL CO., LTD. TSUKUBA PLANT
- Manufacturer Country
- Japan
- Authorized Representative
- KUO'S YUAN IN ENTERPRISE CO., LTD.
Product details
- Intended Use
- 檢測血漿或血清中的D-D雙合蛋白(D-Dimer).
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.7320 Fibrinogen/Fibrinolysis Product Analysis
- Import Information
- import
Dates and status
- Registration Date
- May 03, 2013
- Expiry Date
- May 03, 2018
- Cancellation Date
- Nov 04, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Nanobia D-binary reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 04705a707e02a0af3c7e2595b57ab0b6 and manufactured by SEKISUI MEDICAL CO., LTD. TSUKUBA PLANT. The authorized representative in Taiwan is KUO'S YUAN IN ENTERPRISE CO., LTD..
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