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H4 Cartridge 054330

by Lifehealth

H4 Cartridge 054330 (055704) is a Class II device made by Lifehealth, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00856522006033), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00856522006033 UDI-DI Date24 Sep 2016ListedStatusListed 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  • Withdrawn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
H4 Cartridge
Generic name
Multiple blood gas/haemoximetry/electrolyte analyte IVD, reagent
Model / Ref / Catalog
054330, 055704
Primary DI / UDI-DI
00856522006033
FDA product code
JGS, GKG, CGZ, CEM, CDS
GMDN term
Multiple blood gas/haemoximetry/electrolyte analyte IVD, reagent
Device class
Class II
Regulation number
862.1665, 864.6400, 862.1170, 862.1600, 862.1770
GUDID distribution status
In Commercial Distribution

Related devices

Category: Multiple blood gas/haemoximetry/electrolyte analyte IVD, reagent

Similar devices

Other devices filed under FDA product code JGS (Electrode, Ion Specific, Sodium).

Other devices from Lifehealth

See all devices from Lifehealth →

Properties

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