Taiwan FDA registration b860c9b88dca47dcfdb3c54c93ece6b3
Roche Real-Time Fluorescent EBV Quantitative Test Kit (Unsterilized)
TW: “羅氏”即時螢光EBV定量檢驗試劑套組(未滅菌)
Taiwan·Risk Class 1·CEPHEID AB·Registered Aug 05, 2010 – Aug 05, 2015CancelledRegistration details
- Analysis ID
- b860c9b88dca47dcfdb3c54c93ece6b3
- Customs Code
- DHA04400905103
Company information
- Manufacturer
- CEPHEID AB
- Manufacturer Country
- Sweden
- Authorized Representative
- ROCHE DIAGNOSTICS LTD.
Product details
- Intended Use
- Limited to the first level identification range of "Epstein-Barr virus serum reagent (C.3235)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3235 EB病毒血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Aug 05, 2010
- Expiry Date
- Aug 05, 2015
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Roche Real-Time Fluorescent EBV Quantitative Test Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b860c9b88dca47dcfdb3c54c93ece6b3 and manufactured by CEPHEID AB. The authorized representative in Taiwan is ROCHE DIAGNOSTICS LTD..
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