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WorkMate™ Scribe™ Module

by St. Jude Medical, Inc.

WorkMate™ Scribe™ Module (H702322) is a Class II device made by St. Jude Medical, Inc., listed in FDA GUDID since 13 Sep 2016 (UDI-DI 05415067023223), 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 Number05415067023223 UDI-DI Date13 Sep 2016ListedStatusListed 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  • Withdrawn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
WorkMate™ Scribe™
Generic name
Cardiac catheterization monitoring system
Model / Ref / Catalog
Module, H702322
Primary DI / UDI-DI
05415067023223
FDA product code
DQK
GMDN term
Cardiac catheterization monitoring system
Device class
Class II
Regulation number
870.1425
GUDID distribution status
In Commercial Distribution

Related devices

Category: Cardiac catheterization monitoring system

Similar devices

Other devices filed under FDA product code DQK (COMPUTER, DIAGNOSTIC, PROGRAMMABLE).

Other devices from St. Jude Medical, Inc.

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

Properties

  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)