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MultiCHECK Cardiac 944-514

by Techno-Path Manufacturing

MultiCHECK Cardiac 944-514 is a Class I device made by Techno-Path Manufacturing, listed in FDA GUDID since 16 Sep 2022 (UDI-DI 05391523440158), 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 Number05391523440158 UDI-DI Date16 Sep 2022ListedStatusListed 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  • Withdrawn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
MultiCHECK Cardiac
Generic name
Multiple-type clinical chemistry analyte profile IVD, control
Model / reference
944-514
Primary DI / UDI-DI
05391523440158
FDA product code
JJY, OHQ
GMDN term
Multiple-type clinical chemistry analyte profile IVD, control
Device class
Class I
Regulation number
862.1660
GUDID distribution status
In Commercial Distribution

Related devices

Category: Multiple-type clinical chemistry analyte profile IVD, control

Similar devices in this category

Other devices filed under Multiple-type clinical chemistry analyte profile IVD, control.

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Properties

  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)