Taiwan FDA registration 521cb543c08f431f936d895cd144e5a5
“AGFA”Dentus Film（Non-Sterile）
TW: “艾克發”牙科用X-光軟片（未滅菌）
Taiwan·Risk Class 1·MD·AGFA HEALTHCARE N. V.·Registered Dec 20, 2013 – Dec 20, 2023ExpiredRegistration details
- Analysis ID
- 521cb543c08f431f936d895cd144e5a5
- License Form
- Ministry of Health Medical Device Import No. 013700
- Customs Code
- DHA09401370009
Company information
- Manufacturer
- AGFA HEALTHCARE N. V.
- Manufacturer Country
- Belgium
- Authorized Representative
- ANDLIFE INC.
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
- Dec 20, 2013
- Expiry Date
- Dec 20, 2023
About this record
Access comprehensive regulatory information for “AGFA”Dentus 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 521cb543c08f431f936d895cd144e5a5 and manufactured by AGFA HEALTHCARE N. V.. The authorized representative in Taiwan is ANDLIFE INC..
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