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Corvitals CV1245

by LifeSignals, Inc.

Corvitals CV1245 is a Class II device made by LifeSignals, Inc., listed in FDA GUDID since 26 Jun 2020 (UDI-DI B353CV12451), not in commercial distribution (GUDID) as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB353CV12451 UDI-DI Date26 Jun 2020ListedStatusListed GUDID: not 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  • Withdrawn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
Corvitals
Generic name
Electrocardiography telemetric monitoring system
Model / reference
CV1245
Primary DI / UDI-DI
B353CV12451
FDA product code
MWJ, DRG
GMDN term
Electrocardiography telemetric monitoring system
Device class
Class II
Regulation number
870.2800, 870.2910
GUDID distribution status
Not in Commercial Distribution
MRI safety
MR Unsafe

Similar devices

Other devices filed under FDA product code MWJ (Electrocardiograph, Ambulatory (Without Analysis)).

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)