Taiwan FDA registration 4e6725401c6aab65423157430b68a88e
"LIAISON" XL LAS Analyzer (Non-Sterile)
TW: "禮雅尚"實驗室自動化系統化學冷光免疫分析儀 (未滅菌)
Taiwan·Risk Class 1·MD·DIASORIN S.P.A.·Registered Apr 24, 2019 – Apr 24, 2024CancelledRegistration details
- Analysis ID
- 4e6725401c6aab65423157430b68a88e
- License Form
- Ministry of Health Medical Device Import No. 020364
- Customs Code
- DHA09402036400
Company information
- Manufacturer
- DIASORIN S.P.A.
- Manufacturer Country
- Italy
- 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
- Apr 24, 2019
- Expiry Date
- Apr 24, 2024
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "LIAISON" XL LAS 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 4e6725401c6aab65423157430b68a88e and manufactured by DIASORIN S.P.A.. The authorized representative in Taiwan is MEDRICH INSTRUMENT CO., LTD..
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