Taiwan FDA registration bef8d611053b54cfc9fab1832247ead9
Nitto Spinatomine Propionate Amine Transaminase Reagent (Unsterilized)
TW: 日東紡胺基丙酸胺轉胺酶試劑 (未滅菌)
Taiwan·Risk Class 1·NITTOBO MEDICAL CO., LTD. MEDICAL DEVELOPMENT CENTER·Registered Feb 13, 2020 – Feb 13, 2030ActiveRegistration details
- Analysis ID
- bef8d611053b54cfc9fab1832247ead9
- Customs Code
- DHA09402125602
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- Limited to the classification and grading management method of medical equipment, alanine transaminase test system (A.1030) first level identification range.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1030 丙胺酸轉胺酶試驗系統
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Feb 13, 2020
- Expiry Date
- Feb 13, 2030
About this record
Access comprehensive regulatory information for Nitto Spinatomine Propionate Amine Transaminase 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 bef8d611053b54cfc9fab1832247ead9 and manufactured by NITTOBO MEDICAL CO., LTD. MEDICAL DEVELOPMENT CENTER. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices