Taiwan FDA registration 25a0c8d318a7a58d3e2d365a3849508d
NITTOBO r-GTP (Non-Sterile)
TW: 日東紡 r–麩胺醯轉移酶試劑(未滅菌)
Taiwan·Risk Class 1·MD·NITTOBO MEDICAL CO., LTD. MEDICAL DEVELOPMENT CENTER·Registered Sep 10, 2019 – Sep 10, 2024ExpiredRegistration details
- Analysis ID
- 25a0c8d318a7a58d3e2d365a3849508d
- License Form
- Ministry of Health Medical Device Import No. 020846
- Customs Code
- DHA09402084602
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- Limited to the first level identification range of the measures for the administration of medical devices "r-glutamyl transferase (GGT) and isoenzyme test system (A.1360)".
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1360 r-glutamyl transferase (GGT) and isoenzyme test system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 10, 2019
- Expiry Date
- Sep 10, 2024
About this record
Access comprehensive regulatory information for NITTOBO r-GTP (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 25a0c8d318a7a58d3e2d365a3849508d and manufactured by NITTOBO MEDICAL CO., LTD. MEDICAL DEVELOPMENT CENTER. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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