Confida™ GWBC30
Confida™ GWBC30 is a Class II device made by Medtronic, Inc., cleared under FDA 510(k) K181001 on 3 May 2018 and listed in FDA GUDID since 18 May 2018 (UDI-DI 00763000060886), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00763000060886 | Date18 May 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK181001 | Date3 May 2018 | StatusActive |
Official records
- AccessGUDID record 00763000060886
- FDA 510(k) database K181001
Across registries
- FDA 510(k) K181001 decided 3 May 2018 Active
- FDA GUDID UDI-DI 00763000060886 listed 18 May 2018 Listed
Timeline
- Cleared FDA 510(k) K181001
- Listed FDA GUDID 00763000060886
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Confida™
- Generic name
- Cardiac/peripheral vascular guidewire, single-use
- Model / reference
- GWBC30
- Primary DI / UDI-DI
- 00763000060886
- 510(k) Number
- FDA product code
- DQX
- GMDN term
- Cardiac/peripheral vascular guidewire, single-use
- Device class
- Class II
- Regulation number
- 870.1330
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
- Size
- Length — 260.0 CentimeterOuter Diameter — 0.89 Millimeter
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