Taiwan FDA registration 18c860c87deb2a31fde940617a086d34
"Agfa" radiation video cartridge and sensitization screen
TW: "愛克發" 放射線影片匣及增感屏
Taiwan·Risk Class 2·AGFA-GEVAERT HEALTHCARE GMBH;; AGFA N.V.·Registered Nov 29, 2005 – Nov 29, 2025ExpiredRegistration details
- Analysis ID
- 18c860c87deb2a31fde940617a086d34
- Customs Code
- DHA00601369302
Company information
- Manufacturer
- AGFA-GEVAERT HEALTHCARE GMBH;; AGFA N.V.
- Manufacturer Country
- Belgium;;Germany
- Authorized Representative
- AGFA MATERIALS TAIWAN CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1850 放射線影片匣
- Import Information
- import
Dates and status
- Registration Date
- Nov 29, 2005
- Expiry Date
- Nov 29, 2025
About this record
Access comprehensive regulatory information for "Agfa" radiation video cartridge and sensitization screen in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 18c860c87deb2a31fde940617a086d34 and manufactured by AGFA-GEVAERT HEALTHCARE GMBH;; AGFA N.V.. The authorized representative in Taiwan is AGFA MATERIALS TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices