Fujifilm Automatic Dry Biochemical Analyzer (Unsterilized)
Taiwan·Risk Class 1·FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE·Registered Jun 26, 2012 – Jun 26, 2017Cancelled- Analysis ID
- 39221fcc168208350f7f3181db872356
- Customs Code
- DHA04401187209
- Manufacturer Country
- Japan
- 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
- Input;; QMS/QSD
- Registration Date
- Jun 26, 2012
- Expiry Date
- Jun 26, 2017
- Cancellation Date
- Dec 13, 2019
- Status
- Logged out
- Reason
- 許可證已逾有效期
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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 39221fcc168208350f7f3181db872356 and manufactured by FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE. The authorized representative in Taiwan is HUNG CHONG CORP..
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