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LifeSignals LP1253

by LifeSignals, Inc.

LifeSignals LP1253 (LP1253_US) is a Class II device made by LifeSignals, Inc., listed in FDA GUDID since 28 Jan 2021 (UDI-DI B353LP12531), 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 NumberB353LP12531 UDI-DI Date28 Jan 2021ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
LifeSignals
Generic name
Telemetric electrocardiographic ambulatory recorder
Model / Ref / Catalog
LP1253, LP1253_US
Primary DI / UDI-DI
B353LP12531
FDA product code
DRG, MWJ, QYX
GMDN term
Telemetric electrocardiographic ambulatory recorder
Device class
Class II
Regulation number
870.2910, 870.2800, 870.1025
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Related devices

Category: Electrocardiography telemetric monitoring system

Similar devices

Other devices filed under FDA product code DRG (Transmitters And Receivers, Physiological Signal, Radiofrequency).

Other devices from LifeSignals, Inc.

See all devices from LifeSignals, Inc. →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Serial number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)