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Scribe SCRIBEWS-5BB-YXXXX

by Mortara Instrument, Inc.

Scribe SCRIBEWS-5BB-YXXXX is a Class II device made by Mortara Instrument, Inc., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00812345027372), not in commercial distribution (GUDID) as of 22 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00812345027372 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: not 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  • Withdrawn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
Scribe
Generic name
Electrocardiograph, professional, multichannel
Model / reference
SCRIBEWS-5BB-YXXXX
Primary DI / UDI-DI
00812345027372
FDA product code
DPS, MLO
GMDN term
Electrocardiograph, professional, multichannel
Device class
Class II
Regulation number
870.2340, 870.2800
GUDID distribution status
Not in Commercial Distribution

Other devices from Mortara Instrument, Inc.

See all devices from Mortara Instrument, Inc. →

Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)