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Quickflex™ 1258T

by St. Jude Medical, Inc. 3 variants

Quickflex™ 1258T is a Class III device made by St. Jude Medical, Inc., listed in FDA GUDID since 10 Apr 2017 (UDI-DI 05414734502603), 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 Number05414734502603 UDI-DI Date10 Apr 2017ListedStatusListed 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  • Withdrawn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
Quickflex™
Generic name
Endocardial/interventricular septal pacing lead
Model / Ref / Catalog
1258T
Primary DI / UDI-DI
05414734502603
FDA product code
OJX
GMDN term
Endocardial/interventricular septal pacing lead
Device class
Class III
GUDID distribution status
In Commercial Distribution
Size
Length — 75 Centimeter
Catheter Gauge — 5.0000 French

Related devices

Category: Endocardial/interventricular septal pacing lead

Similar devices

Other devices filed under FDA product code OJX (Drug eluting permanent left ventricular (lv) pacemaker electrode).

Other devices from St. Jude Medical, Inc.

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

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Combination product
  • Serial number
  • Expiration date
Other properties (8, all answered No)