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Catalyst Bariatric Bed ASM100112

by Kreg Medical, Inc.

Catalyst Bariatric Bed ASM100112 is a Class II device made by Kreg Medical, Inc., listed in FDA GUDID since 21 Sep 2018 (UDI-DI 00850520008020), 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 Number00850520008020 UDI-DI Date21 Sep 2018ListedStatusListed 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  • Withdrawn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
Catalyst Bariatric Bed
Generic name
Stand-up bed
Model / reference
ASM100112
Primary DI / UDI-DI
00850520008020
FDA product code
FNL
GMDN term
Stand-up bed
Device class
Class II
Regulation number
880.5100
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FNL (Bed, Ac-Powered Adjustable Hospital).

Other devices from Kreg Medical, Inc.

See all devices from Kreg Medical, Inc. →

Properties

  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)