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Sjm™ 4090/58

by St. Jude Medical, Inc.

Sjm™ 4090/58 is a Class II device made by St. Jude Medical, Inc., listed in FDA GUDID since 23 Nov 2015 (UDI-DI 05414734501637), 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 Number05414734501637 UDI-DI Date23 Nov 2015ListedStatusListed 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  • Withdrawn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

Trade name
Sjm™
Generic name
Pacing/defibrillation lead stylet
Model / Ref / Catalog
4090/58
Primary DI / UDI-DI
05414734501637
FDA product code
DRB
GMDN term
Pacing/defibrillation lead stylet
Device class
Class II
Regulation number
870.1380
GUDID distribution status
In Commercial Distribution
Size
Length — 58 Centimeter

Related devices

Category: Pacing/defibrillation lead stylet

Similar devices

Also classified as Pacing/defibrillation lead stylet.

Similar devices in this category

Other devices filed under Pacing/defibrillation lead stylet.

Other devices from St. Jude Medical, Inc.

See all devices from St. Jude Medical, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)