Evera™ S VR DVBC3D4
Evera™ S VR DVBC3D4 is a Class III device made by Medtronic, Inc., listed in FDA GUDID since 22 May 2017 (UDI-DI 00643169929876), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00643169929876 | Date22 May 2017 | StatusListed |
Official records
- AccessGUDID record 00643169929876
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Evera™ S VR
- Generic name
- Single-chamber implantable defibrillator
- Model / reference
- DVBC3D4
- Primary DI / UDI-DI
- 00643169929876
- FDA product code
- LWS
- GMDN term
- Single-chamber implantable defibrillator
- Device class
- Class III
- GUDID distribution status
- In Commercial Distribution
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