Taiwan FDA registration 0968f7370ca7bf10e55b66c80ffa35ec
"Fujifilm" dental X-ray film (unsterilized)
TW: "富士" 牙科用X光軟片 (未滅菌)
Taiwan·Risk Class 1·YESTAR (GUANGXI) MEDICAL SYSTEM CO., LTD.;; FUJIFILM CORPORATION·Registered Jun 22, 2015 – Jun 22, 2020CancelledRegistration details
- Analysis ID
- 0968f7370ca7bf10e55b66c80ffa35ec
- Customs Code
- DHA09600243100
Company information
- Manufacturer Country
- Japan;;China
- Authorized Representative
- NAN KAI CORPORATION
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Radiographic Film (P.1840)".
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1840 Radiographic film
- Import Information
- Contract manufacturing;; Input;; Chinese goods
Dates and status
- Registration Date
- Jun 22, 2015
- Expiry Date
- Jun 22, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Fujifilm" dental X-ray film (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0968f7370ca7bf10e55b66c80ffa35ec and manufactured by YESTAR (GUANGXI) MEDICAL SYSTEM CO., LTD.;; FUJIFILM CORPORATION. The authorized representative in Taiwan is NAN KAI CORPORATION.
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