Taiwan FDA registration 124b06745162ba35b9d423a358aaacdc
Fujifilm New Automatic Dry Biochemical Analyzer (Unsterilized)
TW: 富士新全自動乾式生化分析儀 (未滅菌)
Taiwan·Risk Class 1·FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE·Registered Dec 12, 2007 – Dec 12, 2017CancelledRegistration details
- Analysis ID
- 124b06745162ba35b9d423a358aaacdc
- Customs Code
- DHA04400638007
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- HUNG CHONG CORP.
Product details
- 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
- import
Dates and status
- Registration Date
- Dec 12, 2007
- Expiry Date
- Dec 12, 2017
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Fujifilm New 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 124b06745162ba35b9d423a358aaacdc 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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