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Horizon Multi-Purpose Stretcher

by GF Health Products, Inc. 2 variants

Ref 462FMCSTModel 462EMCST

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

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

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number++M368HAUSTEDSTRETCHERS6A Basic UDI-DI M368462FMCST1UDI-DIDate30 Sep 2025RegisteredStatusActive
United StatesGUDID listing GUDID NumberM368462FMCST1 UDI-DI Date31 Aug 2016ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Hausted
Generic Name
Hospital stretcher, manual
Model / Reference
462EMCST, 462FMCST
Primary DI / UDI-DI
M368462FMCST1
Basic UDI-DI
++M368HAUSTEDSTRETCHERS6A
Direct Marketing DI
M368462FMCST1
FDA Product Code
FPO
EMDN Code
V08050101 Generic use stretchers
GMDN Term
Hospital stretcher, manual
Device Class
Class I EUDAMED
Class II GUDID
Regulation Number
880.6910
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class I
GUDID
Class II

Manufacturer details

EUDAMED SRN
US-MF-000002167
Authorised representative
CEpartner4U NL-AR-000000111

Other devices from GF Health Products, Inc

See all devices from GF Health Products, Inc →

Properties

  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (21)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No