Taiwan FDA registration a47996cf317a5f63bb3a3307515f59fc
"Mirijia" Illite Electrolyte Analyzer (Non-Sterile)
TW: "美麗佳" 伊利萊特電解質分析儀(未滅菌)
Taiwan·Risk Class 1·MEDICA CORPORATION·Registered Sep 06, 2024 – Sep 06, 2029ActiveRegistration details
- Analysis ID
- a47996cf317a5f63bb3a3307515f59fc
- Customs Code
- DHA09402359505
Company information
- Manufacturer
- MEDICA CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- GRAND MARQUIS CO., LTD.
Product details
- Intended Use
- It is limited to the first-level identification scope of the "Clinical Chemical Ion Analyzer (A.0002)" Administrative Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.0002 Clinicalized Molecule Analyzer
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Sep 06, 2024
- Expiry Date
- Sep 06, 2029
About this record
Access comprehensive regulatory information for "Mirijia" Illite Electrolyte 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 a47996cf317a5f63bb3a3307515f59fc and manufactured by MEDICA CORPORATION. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..
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