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Sprint Quattro Secure® Dxac/Dsp 694758

by Medtronic, Inc.

Ref 694758

Active European Union. Also listed in GUDID (US), not in commercial distribution.

CE MDD CE AIMDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/AIMDD EUDAMED NumberB-00721902251917 Basic UDI-DI 00721902251917UDI-DIDate28 Sep 2026RegisteredStatusActive
European UnionCE/MDD EUDAMED NumberB-00721902251917 Basic UDI-DI 00721902251917UDI-DIDate28 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00721902251917 UDI-DI Date26 Nov 2014ListedStatusListed GUDID: not in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/AIMDD, CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Sprint Quattro Secure® EUDAMED
Sprint Quattro Secure® Dxac/Dsp GUDID
Generic Name
Endocardial defibrillation lead
Device Name
Defibrillation Lead
Model / Reference
694758
Primary DI / UDI-DI
00721902251917 EUDAMED
00643169535961 GUDID
Basic UDI-DI
B-00721902251917
FDA Product Code
NVY, DTB, LWS
EMDN Code
J019001020102 Permanent cardiac defibrillator leads, double coil
GMDN Term
Endocardial defibrillation lead
Device Class
Class AIMDD EUDAMED
Class III GUDID
Regulation Number
870.3680
EU market of registration
Netherlands
GUDID distribution status
Not in Commercial Distribution
Size
Length — 58.0 Centimeter

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
00721902251917
GUDID
00643169535961
Device ClassEUDAMED
Class AIMDD
GUDID
Class III

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Properties

  • Sterile
  • Single Use
  • Implantable
  • Incorporates Medicinal Product
  • Prescription Use
  • Combination Product
  • Serial Number

Other properties (17)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No