Taiwan FDA registration 885bcffc7c4bf0de89ba80b6f5084c68
Roche immunoassay vitamin D total analysis test reagent third generation
TW: 羅氏免疫分析維生素D總量分析檢驗試劑第三代
Taiwan·Risk Class 2·ROCHE DIAGNOSTICS GMBH·Registered Jul 05, 2022 – Jul 05, 2027ActiveRegistration details
- Analysis ID
- 885bcffc7c4bf0de89ba80b6f5084c68
- Customs Code
- DHA05603567104
Company information
- Manufacturer
- ROCHE DIAGNOSTICS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- ROCHE DIAGNOSTICS LTD.
Product details
- Intended Use
- For details, please refer to the approved version of the Chinese manual.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1825 維他命D試驗系統;; A.1660 Grade Material (Analysis Material Non-Analysis);; A.1150 Calibrated Products
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jul 05, 2022
- Expiry Date
- Jul 05, 2027
About this record
Access comprehensive regulatory information for Roche immunoassay vitamin D total analysis test reagent third generation in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 885bcffc7c4bf0de89ba80b6f5084c68 and manufactured by ROCHE DIAGNOSTICS GMBH. The authorized representative in Taiwan is ROCHE DIAGNOSTICS LTD..
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