Taiwan FDA registration ef2f33f065a65969a9bd6f75cd6340f4
"CDR" Radiologic Patient Cradle (Non-Sterile)
TW: "希迪爾"放射科病患用支架(未滅菌)
Taiwan·Risk Class 1·MD·CDR Systems Inc.·Registered May 06, 2019 – May 06, 2024ExpiredRegistration details
- Analysis ID
- ef2f33f065a65969a9bd6f75cd6340f4
- License Form
- Ministry of Health Medical Device Import No. 020403
- Customs Code
- DHA09402040307
Company information
- Manufacturer
- CDR Systems Inc.
- Manufacturer Country
- Canada
- Authorized Representative
- Yaukang international 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
- May 06, 2019
- Expiry Date
- May 06, 2024
About this record
Access comprehensive regulatory information for "CDR" 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 ef2f33f065a65969a9bd6f75cd6340f4 and manufactured by CDR Systems Inc.. The authorized representative in Taiwan is Yaukang international 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