Taiwan FDA registration 78f5a4fd461a75ccaf87364bac6ffb55
"Abbott" Alinity i Insulin Reagent Kit(Non-Sterile)
TW: "亞培" 胰島素檢驗試劑組(未滅菌)
Taiwan·Risk Class 1·MD·DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY·Registered Jun 15, 2018 – Jun 15, 2023ExpiredRegistration details
- Analysis ID
- 78f5a4fd461a75ccaf87364bac6ffb55
- License Form
- Ministry of Health Medical Device Import No. 019190
- Customs Code
- DHA09401919003
Company information
- Manufacturer
- DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- Limited to the first level identification range of the immunoresponsive insulin test system (A.1405) of the management method for medical devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1405 Immunoresponsive Insulin Test System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 15, 2018
- Expiry Date
- Jun 15, 2023
About this record
Access comprehensive regulatory information for "Abbott" Alinity i Insulin 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 78f5a4fd461a75ccaf87364bac6ffb55 and manufactured by DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
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