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5873W

by Medtronic, Inc. 2 variants

5873W is a Class I device made by Medtronic, Inc., listed in FDA GUDID since 11 Mar 2024 (UDI-DI 00763000812065), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00763000812065 UDI-DI Date11 Mar 2024ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name
Pacing/defibrillation lead repair kit
Model / reference
5873W
Primary DI / UDI-DI
00763000812065
FDA product code
DTF
GMDN term
Pacing/defibrillation lead repair kit
Device class
Class I
Regulation number
870.3730
GUDID distribution status
In Commercial Distribution

Related devices

Category: Pacing/defibrillation lead repair kit

Other devices from Medtronic, Inc.

See all devices from Medtronic, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
Other properties (9, all answered No)