Fujifilm Automatic Dry Biochemical Analyzer (Unsterilized)
Taiwan·Risk Class 1·FUJIFILM IMAGING SYSTEMS (SUZHOU) CO., LTD.·Registered Jul 08, 2013 – Jul 08, 2018Cancelled- Analysis ID
- af875f933410e4a4c3ffe5b65295e62c
- Customs Code
- DHA04600192807
- Manufacturer
- FUJIFILM IMAGING SYSTEMS (SUZHOU) CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- HUNG CHONG CORP.
- Intended Use
- Limited to the first level identification range of the "Individual Photometric Chemical Analyzer for Clinical Use (A.2160)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2160 Individual Photometric Chemistry Analyzer for Clinical Use
- Import Information
- Chinese goods;; Input;; QMS/QSD
- Registration Date
- Jul 08, 2013
- Expiry Date
- Jul 08, 2018
- Cancellation Date
- Jul 15, 2022
- Status
- Logged out
- Reason
- 未展延而逾期者
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Access comprehensive regulatory information for Fujifilm Automatic Dry Biochemical Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number af875f933410e4a4c3ffe5b65295e62c and manufactured by FUJIFILM IMAGING SYSTEMS (SUZHOU) CO., LTD.. The authorized representative in Taiwan is HUNG CHONG CORP..
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