Skip to content

Na 3111

by St. Jude Medical, Inc. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05414734507004 UDI-DIDate30 Apr 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Generic Name
Cardiac pulse generator test magnet
Model / Ref / Catalog
3111
Primary DI / UDI-DI
05414734507004
FDA Product Code
DTG
GMDN Term
Cardiac pulse generator test magnet
Device Class
Class I
Regulation Number
870.3690
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 3.0000 Inch

Related devices

Category: Cardiac pulse generator test magnet

Other devices from St. Jude Medical, Inc.

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

Properties

  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No