Taiwan FDA registration ca7690d7d314ae0a5f469536dd570f46
"Artron" Helicobacter Pylori Reagents (Non-sterile)
TW: "雅創" 幽門桿菌試劑 (未滅菌)
Taiwan·Risk Class 1·MD·ARTRON LABORATORIES INC.·Registered Mar 07, 2018 – Mar 07, 2023ExpiredRegistration details
- Analysis ID
- ca7690d7d314ae0a5f469536dd570f46
- License Form
- Ministry of Health Medical Device Import No. 018873
- Customs Code
- DHA09401887300
Company information
- Manufacturer
- ARTRON LABORATORIES INC.
- Manufacturer Country
- Canada
- Authorized Representative
- GORED ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Helicobacter Serological Reagent (C.0003)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C0003 Helicobacter serological reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 07, 2018
- Expiry Date
- Mar 07, 2023
About this record
Access comprehensive regulatory information for "Artron" Helicobacter Pylori Reagents (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 ca7690d7d314ae0a5f469536dd570f46 and manufactured by ARTRON LABORATORIES INC.. The authorized representative in Taiwan is GORED ENTERPRISE 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