Taiwan FDA registration 6e0530cebe8f3258f363eeb5c8a2fa53
“Qfix” Radiologic Patient Cradle (Non-Sterile)
TW: “科輔適”放射科病患用支架(未滅菌)
Taiwan·Risk Class 1·MD·QFIX·Registered Oct 01, 2013 – Oct 01, 2028ActiveRegistration details
- Analysis ID
- 6e0530cebe8f3258f363eeb5c8a2fa53
- License Form
- Ministry of Health Medical Device Import No. 013467
- Customs Code
- DHA09401346703
Company information
- Manufacturer
- QFIX
- Manufacturer Country
- United States
- Authorized Representative
- Varian Medical Systems Taiwan Co., Ltd.
Product details
- Intended Use
- Limited to the first-level identification range of the Measures for the Administration of Medical Equipment "Stent for Radiology Patients (P.1830)".
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1830 Stent for radiology patients
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2013
- Expiry Date
- Oct 01, 2028
About this record
Access comprehensive regulatory information for “Qfix” Radiologic Patient Cradle (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 6e0530cebe8f3258f363eeb5c8a2fa53 and manufactured by QFIX. The authorized representative in Taiwan is Varian Medical Systems 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