Vv-Plug
by Oscor Inc.
Ref VV-PLUGModel VV
Vv-Plug is a Class III device made by Oscor Inc., registered in EUDAMED on 20 Oct 2026 (Basic UDI-DI B-00836559002857), cleared under FDA 510(k) K862966 on 31 Oct 1986 and listed in FDA GUDID since 16 Oct 2015 (UDI-DI 00836559002857), active as of 24 Oct 2026.
Active
CE MDD 510(k)
Valid until
No date given
FDA recalls
None found
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-00836559002857 00836559002857 | Date20 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00836559002857 | Date16 Oct 2015 | StatusListed |
| United States | FDA 510(k)SESE GUDID | NumberK862966 | Date31 Oct 1986 | StatusActive |
Official records
- EUDAMED public site B-00836559002857
- AccessGUDID record 00836559002857
- FDA 510(k) database K862966
Across registries
- EUDAMED Basic UDI-DI B-00836559002857 registered 20 Oct 2026 Active
- FDA 510(k) K862966 decided 31 Oct 1986 Active
- FDA GUDID UDI-DI 00836559002857 listed 16 Oct 2015 Listed
Timeline
- Cleared FDA 510(k) K862966
- Listed FDA GUDID 00836559002857
- Registered EUDAMED B-00836559002857
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Port Plug EUDAMEDVv-Plug GUDID
- Generic name
- Implantable pulse generator port plug
- Model / Ref / Catalog
- VV-PLUG, VV
- Primary DI / UDI-DI
- 00836559002857
- Basic UDI-DI
- B-00836559002857
- 510(k) Number
- FDA product code
- DTB
- EMDN code
- C020180 Cardiac electrophysiology and mapping devices - accessories
- GMDN term
- Implantable pulse generator port plug
- Device class
- Class III
- Regulation number
- 870.3680
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
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