Taiwan FDA registration 87152a736959454c242df40d8e14fd14
Nitto Spinning Ammonia Liquid Reagent (unsterilized)
TW: 日東紡氨液狀試劑（未滅菌）
Taiwan·Risk Class 1·NITTOBO MEDICAL CO., LTD. MEDICAL DEVELOPMENT CENTER·Registered Dec 20, 2010 – Dec 20, 2025ExpiredRegistration details
- Analysis ID
- 87152a736959454c242df40d8e14fd14
- Customs Code
- DHA04400970804
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- It is limited to the first-level identification scope of the "Blood Ammonia Test System (A.1065)" of the Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1065 血氨試驗系統
- Import Information
- import
Dates and status
- Registration Date
- Dec 20, 2010
- Expiry Date
- Dec 20, 2025
About this record
Access comprehensive regulatory information for Nitto Spinning Ammonia Liquid Reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 87152a736959454c242df40d8e14fd14 and manufactured by NITTOBO MEDICAL CO., LTD. MEDICAL DEVELOPMENT CENTER. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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