Taiwan FDA registration 5096bba76c58162be9efbc1d15cec312

"Damon" electrolyte analyzer (non-sterile)

TW: "戴蒙" 電解質分析儀(未滅菌)

Taiwan·Risk Class 1·Diamond Diagnostics Inc.·Registered Jun 19, 2024 – Jun 19, 2029Active

Registration details

Analysis ID: 5096bba76c58162be9efbc1d15cec312
Customs Code: DHA09402351507

Company information

Manufacturer: Diamond Diagnostics Inc.
Manufacturer Country: United States
Authorized Representative: EAFAN ENTERPRISE 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: Jun 19, 2024
Expiry Date: Jun 19, 2029

About this record

Access comprehensive regulatory information for "Damon" 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 5096bba76c58162be9efbc1d15cec312 and manufactured by Diamond Diagnostics Inc.. The authorized representative in Taiwan is EAFAN ENTERPRISE CO., LTD..

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