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Progressa® Surface P7520A2S

by Hill-Rom, Inc.

Progressa® Surface P7520A2S is a Class II device made by Hill-Rom, Inc., listed in FDA GUDID since 17 Sep 2016 (UDI-DI 00887761999787), 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 Number00887761999787 UDI-DI Date17 Sep 2016ListedStatusListed 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  • Withdrawn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
Progressa® Surface
Generic name
Alternating-pressure bed mattress overlay system
Model / reference
P7520A2S
Primary DI / UDI-DI
00887761999787
FDA product code
IOQ, FNL
GMDN term
Alternating-pressure bed mattress overlay system
Device class
Class II
Regulation number
890.5170, 880.5100
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Similar devices

Other devices filed under FDA product code IOQ (BED, FLOTATION THERAPY, POWERED).

Other devices from Hill-Rom, Inc.

See all devices from Hill-Rom, Inc. →

Properties

  • Serial number
  • Manufacturing date
Other properties (13, all answered No)