Taiwan FDA registration bf202f983148ca7e1aa6851d8958063a
"LIAISON" XL Analyzer (Non-Sterile)
TW: "禮雅尚" 全自動冷光免疫分析儀 (未滅菌)
Taiwan·Risk Class 1·MD·DIASORIN DEUTSCHLAND GMBH·Registered Mar 08, 2017 – Mar 08, 2022CancelledRegistration details
- Analysis ID
- bf202f983148ca7e1aa6851d8958063a
- License Form
- Ministry of Health Medical Device Import No. 017573
- Customs Code
- DHA09401757309
Company information
- Manufacturer
- DIASORIN DEUTSCHLAND GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- MEDRICH INSTRUMENT CO., LTD.
Product details
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A2160 Individual photometric chemistry analyzer for clinical use
- Import Information
- Imported from abroad; GMP
Dates and status
- Registration Date
- Mar 08, 2017
- Expiry Date
- Mar 08, 2022
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "LIAISON" XL Analyzer (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 bf202f983148ca7e1aa6851d8958063a and manufactured by DIASORIN DEUTSCHLAND GMBH. The authorized representative in Taiwan is MEDRICH INSTRUMENT 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