Taiwan FDA registration 6260943a86e0a51b6287bec5a2800855
Bayernix Radiology Patient Positioning Stent (Unsterilized)
TW: “拜耳尼克斯”放射科病患定位用支架 （未滅菌）
Taiwan·Risk Class 1·BIONIX DEVELOPMENT CORPORATION·Registered Aug 31, 2006 – Aug 31, 2011CancelledRegistration details
- Analysis ID
- 6260943a86e0a51b6287bec5a2800855
- Customs Code
- DHA04400510901
Company information
- Manufacturer
- BIONIX DEVELOPMENT CORPORATION
- Manufacturer Country
- United States
- 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
- import
Dates and status
- Registration Date
- Aug 31, 2006
- Expiry Date
- Aug 31, 2011
- Cancellation Date
- Nov 30, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Bayernix Radiology Patient Positioning Stent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6260943a86e0a51b6287bec5a2800855 and manufactured by BIONIX DEVELOPMENT CORPORATION. The authorized representative in Taiwan is Cypper Enterprises Limited.
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