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M24 Hematocrit Centrifuge, 220v HEC-24HF-7502

by Lw Scientific, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00664816002513 UDI-DI Date1 Aug 2016ListedStatusListed 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  • Withdrawn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
M24 Hematocrit Centrifuge, 220v
Generic Name
Microhaematocrit centrifuge IVD
Model / Reference
HEC-24HF-7502
Primary DI / UDI-DI
00664816002513
FDA Product Code
GKG
GMDN Term
Microhaematocrit centrifuge IVD
Device Class
Class II
Regulation Number
864.6400
GUDID distribution status
Not in Commercial Distribution

Other devices from Lw Scientific, Inc.

See all devices from Lw Scientific, Inc. →

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Expiration Date: No
  • Manufacturing Date: No