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HScribe HSREV-AAA-BXXAA

by Mortara Instrument, Inc.

HScribe HSREV-AAA-BXXAA is a Class II device made by Mortara Instrument, Inc., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00812345027280), 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 Number00812345027280 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  • Withdrawn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
HScribe
Generic name
Electrocardiographic long-term ambulatory recording analyser application software
Model / reference
HSREV-AAA-BXXAA
Primary DI / UDI-DI
00812345027280
FDA product code
MLO
GMDN term
Electrocardiographic long-term ambulatory recording analyser application software
Device class
Class II
Regulation number
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)