Taiwan FDA registration 7e0b7e39713962ccf0973ab1fd29cb52
“Abbott” A-1-AGP Reagent Kit (Non-Sterile)
TW: “亞培” α-1-酸性醣蛋白試劑 (未滅菌)
Taiwan·Risk Class 1·MD·BIOKIT S.A.·Registered Aug 09, 2018 – Aug 09, 2028ActiveRegistration details
- Analysis ID
- 7e0b7e39713962ccf0973ab1fd29cb52
- License Form
- Ministry of Health Medical Device Import No. 019473
- Customs Code
- DHA09401947302
Company information
- Manufacturer
- BIOKIT S.A.
- Manufacturer Country
- Spain
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- Limited to the first level identification range of the medical device management method α-1-glycoprotein immunoassay system (C.5420).
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C5420 α-1-glycoprotein immunoassay system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 09, 2018
- Expiry Date
- Aug 09, 2028
About this record
Access comprehensive regulatory information for “Abbott” A-1-AGP Reagent 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 7e0b7e39713962ccf0973ab1fd29cb52 and manufactured by BIOKIT S.A.. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
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