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Allen 107002

by Hill-Rom, Inc. 17 variants

Allen 107002 (O-ABRC) is a Class I device made by Hill-Rom, Inc., listed in FDA GUDID since 26 May 2023 (UDI-DI 00615521019198), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00615521019198 UDI-DI Date26 May 2023ListedStatusListed 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  • Withdrawn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
Allen
Generic name
Arm procedure positioner, reusable
Model / Ref / Catalog
107002, O-ABRC
Primary DI / UDI-DI
00615521019198
FDA product code
FWZ
GMDN term
Arm procedure positioner, reusable
Device class
Class I
Regulation number
878.4950
GUDID distribution status
In Commercial Distribution

Related devices

Category: Arm procedure positioner, reusable

Similar devices in this category

Other devices filed under Arm procedure positioner, reusable.

Other devices from Hill-Rom, Inc.

See all devices from Hill-Rom, Inc. →

Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)