Taiwan FDA registration 9569dd6837a539c0acb7d935d293e617
cobas HPV
TW: 羅氏可霸斯全自動人類乳突病毒核酸檢驗組
Taiwan·Risk Class 3·MD·ROCHE MOLECULAR SYSTEMS, INC.·Registered Nov 25, 2019 – Nov 25, 2024ExpiredRegistration details
- Analysis ID
- 9569dd6837a539c0acb7d935d293e617
- License Form
- Ministry of Health Medical Device Import No. 032970
- Customs Code
- DHA05603297002
Company information
- Manufacturer
- ROCHE MOLECULAR SYSTEMS, INC.
- Manufacturer Country
- United States
- 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)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C0004 Human papillomavirus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 25, 2019
- Expiry Date
- Nov 25, 2024
About this record
Access comprehensive regulatory information for cobas HPV in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 9569dd6837a539c0acb7d935d293e617 and manufactured by ROCHE MOLECULAR SYSTEMS, INC.. The authorized representative in Taiwan is ROCHE DIAGNOSTICS LTD..
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