Skip to content

Armboard Pad

by Steris Corporation 2 variants

Armboard Pad (P150832815) is a Class I device made by Steris Corporation, listed in FDA GUDID since 17 Nov 2023 (UDI-DI 00724995216542), 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 Number00724995216542 UDI-DI Date17 Nov 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  • Withdrawn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

Generic name
Operating table mattress, basic
Model / Ref / Catalog
Armboard Pad, P150832815
Description
The 5085SRT Featherweight Leg Section Pad Set used with the STERIS 5085SRT Surgical Tables.
Primary DI / UDI-DI
00724995216542
FDA product code
LWG
GMDN term
Operating table mattress, basic
Device class
Class I
Regulation number
878.4950
GUDID distribution status
In Commercial Distribution

Related devices

Category: Operating table mattress, basic

Similar devices in this category

Other devices filed under Operating table mattress, basic.

Other devices from Steris Corporation

See all devices from Steris Corporation →

Properties

  • Over-the-counter
  • Premarket exempt
  • Manufacturing date
Other properties (12, all answered No)