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Amerilux ALX36M

by GF Health Products, Inc.

Amerilux ALX36M is a Class II device made by GF Health Products, Inc., listed in FDA GUDID since 29 Oct 2026 (UDI-DI M368ALX36M1), registry data as of 9 Nov 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberM368ALX36M1 UDI-DI Date29 Oct 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  • Withdrawn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
Amerilux
Generic name
Basic electric hospital bed
Model / reference
ALX36M
Primary DI / UDI-DI
M368ALX36M1
FDA product code
FNL
GMDN term
Basic electric hospital bed
Device class
Class II
Regulation number
880.5100
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 (13, all answered No)