Taiwan FDA registration bf310baeef6e751e5a11bb7fb1a5e4b0
"Agfa” CEA Radiographic Film (Non-Sterile)
TW: “愛克發”喜悅醫用X光軟片 (未滅菌)
Taiwan·Risk Class 1·MD·AGFA N.V.·Registered Nov 01, 2018 – Nov 01, 2028ActiveRegistration details
- Analysis ID
- bf310baeef6e751e5a11bb7fb1a5e4b0
- License Form
- Ministry of Health Medical Device Import No. 019760
- Customs Code
- DHA09401976005
Company information
- Manufacturer
- AGFA N.V.
- Manufacturer Country
- Belgium
- Authorized Representative
- AGFA MATERIALS TAIWAN CO., LTD.
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 Devices for radiology
- Product Type (Level 2)
- P1840 Radiographic video
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 01, 2018
- Expiry Date
- Nov 01, 2028
About this record
Access comprehensive regulatory information for "Agfa” CEA Radiographic Film (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bf310baeef6e751e5a11bb7fb1a5e4b0 and manufactured by AGFA N.V.. The authorized representative in Taiwan is AGFA MATERIALS TAIWAN CO., LTD..
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