Taiwan FDA registration 0847e498c8035e6c97a4251863395e02
“Medica” Blood Gas and Electrolyte Quality Control (Non-Sterile)
TW: “美麗佳”血液氣體電解質品管材料 (未滅菌)
Taiwan·Risk Class 1·MD·MEDICA CORPORATION·Registered Nov 28, 2018 – Nov 28, 2023ExpiredRegistration details
- Analysis ID
- 0847e498c8035e6c97a4251863395e02
- License Form
- Ministry of Health Medical Device Import No. 019859
- Customs Code
- DHA09401985901
Company information
- Manufacturer
- MEDICA CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- GRAND MARQUIS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of quality control materials (analytical and non-analytical) (A.1660) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1660 Quality Control Materials (Analytical and Non-Analytical)
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 28, 2018
- Expiry Date
- Nov 28, 2023
About this record
Access comprehensive regulatory information for “Medica” Blood Gas and Electrolyte Quality Control (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 0847e498c8035e6c97a4251863395e02 and manufactured by MEDICA CORPORATION. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..
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