Taiwan FDA registration e69ac2f536d7e46f4d01f9fbf514dcd1
"Sieber" Radiology Patient Positioning Stent Equipment (Unsterilized)
TW: “希柏”放射科病患定位用支架器材 (未滅菌)
Taiwan·Risk Class 1·BLESSING CATHAY CORPORATION·Registered Sep 28, 2012 – Sep 28, 2017CancelledRegistration details
- Analysis ID
- e69ac2f536d7e46f4d01f9fbf514dcd1
Company information
- Manufacturer
- BLESSING CATHAY CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Cypper Enterprises Limited
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 Radiology Science
- Product Type (Level 2)
- P.1830 放射科病患用支架
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Sep 28, 2012
- Expiry Date
- Sep 28, 2017
- Cancellation Date
- Aug 16, 2017
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Sieber" Radiology Patient Positioning Stent Equipment (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e69ac2f536d7e46f4d01f9fbf514dcd1 and manufactured by BLESSING CATHAY CORPORATION. The authorized representative in Taiwan is Cypper Enterprises Limited.
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