Taiwan FDA registration c18dbb19ddf483b6fba3be0bc03fc4f9
"Carestream" Radiographic Intensifying Screen (Non-Sterile)
TW: "康世" 放射線強化螢幕 (未滅菌)
Taiwan·Risk Class 1·MD·CARESTREAM HEALTH, INC.·Registered May 04, 2017 – May 04, 2022ExpiredRegistration details
- Analysis ID
- c18dbb19ddf483b6fba3be0bc03fc4f9
- License Form
- Ministry of Health Medical Device Import No. 017790
- Customs Code
- DHA09401779004
Company information
- Manufacturer
- CARESTREAM HEALTH, INC.
- Manufacturer Country
- United States
- Authorized Representative
- FAITH BIOMED LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Radiation Enhanced Screen (P.1960)".
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1960 Radiation Enhancement Screen
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 04, 2017
- Expiry Date
- May 04, 2022
About this record
Access comprehensive regulatory information for "Carestream" Radiographic Intensifying Screen (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 c18dbb19ddf483b6fba3be0bc03fc4f9 and manufactured by CARESTREAM HEALTH, INC.. The authorized representative in Taiwan is FAITH BIOMED LTD..
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