Taiwan FDA registration 301ab772b06f224b59c8c95cd19d6c22
"Roche" negative quality tube probe (unsterilized)
TW: "羅氏" 陰性品管探針(未滅菌)
Taiwan·Risk Class 1·VENTANA MEDICAL SYSTEMS, INC.·Registered Jan 11, 2023 – Jan 11, 2028ActiveRegistration details
- Analysis ID
- 301ab772b06f224b59c8c95cd19d6c22
- Customs Code
- DHA09402300905
Company information
- Manufacturer
- VENTANA MEDICAL SYSTEMS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ROCHE DIAGNOSTICS LTD.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment, quality control materials (analytical and non-analytical) (A.1660) the first level identification range.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Quality control materials (analytical and non-analytical)
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jan 11, 2023
- Expiry Date
- Jan 11, 2028
About this record
Access comprehensive regulatory information for "Roche" negative quality tube probe (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 301ab772b06f224b59c8c95cd19d6c22 and manufactured by VENTANA MEDICAL SYSTEMS, INC.. The authorized representative in Taiwan is ROCHE DIAGNOSTICS LTD..
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