Taiwan FDA registration 2b6797d8add776d7ecfeb2ab88982db5
Nitto Spinbo aspartine transferase reagent
TW: 日東紡天門冬胺酸轉移酶試劑
Taiwan·Risk Class 2·NITTOBO MEDICAL CO., LTD. MEDICAL DEVELOPMENT CENTER·Registered Dec 27, 2019 – Dec 27, 2024CancelledRegistration details
- Analysis ID
- 2b6797d8add776d7ecfeb2ab88982db5
- Customs Code
- DHA05603311901
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- This product is used to determine the activity of aspartine transferase AST (also known as GOT) in serum or plasma.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1100 天門冬胺酸轉胺酶試驗系統
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Dec 27, 2019
- Expiry Date
- Dec 27, 2024
- Cancellation Date
- Oct 16, 2024
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Nitto Spinbo aspartine transferase reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2b6797d8add776d7ecfeb2ab88982db5 and manufactured by NITTOBO MEDICAL CO., LTD. MEDICAL DEVELOPMENT CENTER. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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