Visia AF™
Ref DVAC3D1
Visia AF™ (DVAC3D1) is a device classified as Active implantable (AIMDD) made by Medtronic, Inc., registered in EUDAMED on 26 Aug 2026 (Basic UDI-DI B-00763000052713), active as of 24 Oct 2026.
Active
CE AIMDD
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/AIMDD | NumberB-00763000052713 | Date26 Aug 2026 | StatusActive |
Official records
- EUDAMED public site B-00763000052713
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/AIMDD Active
Specification
- Device name
- Evera,Visia AF, Primo/Mirro w MRI
- Model / reference
- DVAC3D1
- Primary DI / UDI-DI
- 00763000052713, 00643169566392
- Basic UDI-DI
- B-00763000052713, B-00643169566392
- EMDN code
- J01050101 Implantable single chamber defibrillators, with sensors
- Device class
- Class AIMDD
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Netherlands
Manufacturer details
- EUDAMED SRN
- US-MF-000019977
- Authorised representative
- Medtronic B.V. NL-AR-000006050
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