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Hausted 5600-Fl-Ar

by GF Health Products, Inc

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberM3685600FLAR1 UDI-DI Date16 Sep 2026ListedStatusListed GUDID: 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  • Withdrawn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
Hausted
Generic Name
Examination/treatment table, line-powered
Model / Reference
5600-FL-AR
Primary DI / UDI-DI
M3685600FLAR1
FDA Product Code
LGX
GMDN Term
Examination/treatment table, line-powered
Device Class
Class I
Regulation Number
878.4960
GUDID distribution status
In Commercial Distribution

Other devices from GF Health Products, Inc

See all devices from GF Health Products, Inc →

Properties

  • Premarket Exempt
  • Serial Number

Other properties (12)

  • 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
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No