Transvene®
Ref 6937-110
Transvene® (6937-110) is a device classified as Active implantable (AIMDD) made by Medtronic, Inc., registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI B-00681490743303), active as of 7 Nov 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-00681490743303 | Date29 Oct 2026 | StatusActive |
Official records
- EUDAMED public site B-00681490743303
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/AIMDD Active
Specification
- Device name
- 6937 TRANSVENE Lead
- Model / reference
- 6937-110
- Primary DI / UDI-DI
- 00681490743303, 00763000009427, 00613994492463, 00681490743310, 00613994551917, 00613994551924
- Basic UDI-DI
- B-00681490743303, B-00763000009427, B-00613994492463, B-00681490743310, B-00613994551917, B-00613994551924
- EMDN code
- J019001020101 Permanent cardiac defibrillator leads, single coil
- 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
Similar devices in this category
Other devices filed under PERMANENT CARDIAC LEADS.
- EMBLEM™ 3501 by Cardiac Pacemakers, Inc., a subsidiary of Boston Scientific Corporation
- Lead Adaptor BIS/BIS-40 by Oscor Inc.
- Lead Adaptor 664403-302 BLV/BIS-4403 by Oscor Inc.
- Crystalline® ICQ09B58 by Vitatron Holding BV
- Tendril MRI™ LPA1200M-58 by ST. JUDE MEDICAL, INC.
- NAVIGO 4LV ARC 88 TLT022C by MicroPort CRM S.r.l.
- EMBLEM™ 4712 by Cardiac Pacemakers, Inc., a subsidiary of Boston Scientific Corporation
- NAVIGO 4LV 2D 78 TLT019C by MicroPort CRM S.r.l.
- Crystalline® ICF09B52 by Vitatron Holding BV