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Creatinine Control Kit 074446

by Lifehealth

Creatinine Control Kit 074446 (074402) is a Class I device made by Lifehealth, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00856522006095), 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 Number00856522006095 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  • Withdrawn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
Creatinine Control Kit
Generic name
Creatinine IVD, control
Model / Ref / Catalog
074446, 074402
Primary DI / UDI-DI
00856522006095
FDA product code
JJX
GMDN term
Creatinine IVD, control
Device class
Class I
Regulation number
862.1660
GUDID distribution status
In Commercial Distribution

Related devices

Category: Creatinine IVD, control

Similar devices

Other devices filed under FDA product code JJX (Single (Specified) Analyte Controls (Assayed And Unassayed)).

Other devices from Lifehealth

See all devices from Lifehealth →

Properties

  • Single use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)