Taiwan FDA registration 64805dd58b523250ad39c0f5f3ca8113
"Trinity" 6-Phosphogluconate dehydrogenase Kit (Non-sterile)
TW: "保成" 6-磷糖去氫酵素檢驗試劑 (未滅菌)
Registration details
- Analysis ID
- 64805dd58b523250ad39c0f5f3ca8113
- License Form
- Ministry of Health Medical Device Import No. 022099
- Customs Code
- DHA09402209901
Company information
- Manufacturer
- Trinity Biotech Plc
- Manufacturer Country
- Ireland
- Authorized Representative
- BioChain Co., Ltd.
Product details
- Intended Use
- Limited to the first level identification range of the 6-phosphose dehydrogenase test system (A.1565) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1565 6-Phosphosyldehydrogenase test system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 10, 2020
- Expiry Date
- Nov 10, 2025
About this record
Access comprehensive regulatory information for "Trinity" 6-Phosphogluconate dehydrogenase Kit (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 64805dd58b523250ad39c0f5f3ca8113 and manufactured by Trinity Biotech Plc. The authorized representative in Taiwan is BioChain Co., Ltd..
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