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Compella™Bariatric Bed P7800A

by Hill-Rom, Inc.

Ref P7800

Compella™Bariatric Bed P7800A is a device classified as Class IIa in the EU and Class II in the US made by Hill-Rom, Inc., registered in EUDAMED on 12 Jun 2026 (Basic UDI-DI 0887761GMN000062UA) with CE/MDR certificate 1000316858 valid until 3 May 2031 and listed in FDA GUDID since 17 Sep 2016 (UDI-DI 00887761000902), active as of 22 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

3 May 2031

CE MDR certificate

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

1 certificate

Certifier DQS Medizinprodukte GmbH

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0887761GMN000062UA Basic UDI-DI 00887761000902UDI-DIDate12 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00887761000902 UDI-DI Date17 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0887761GMN000062UA registered 12 Jun 2026 Active· +1 more in the status table
  • FDA GUDID UDI-DI 00887761000902 listed 17 Sep 2016 Listed

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 1000316858 Active Amended

    Quality management system EU MDR

    Certifier
    DQS Medizinprodukte GmbH 0297
    Issued
    3 Jun 2026
    Expires
    3 May 2031
    Reason
    Ar data change

Timeline

4 dated events

  1. Listed FDA GUDID 00887761000902
  2. Certificate issued EUDAMED 1000316858
  3. Registered EUDAMED 0887761GMN000062UA
  4. Certificate expires EUDAMED 1000316858

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Compella EUDAMED
Compella™Bariatric Bed GUDID
Generic name
Bariatric bed
Model / reference
P7800 EUDAMED
P7800A GUDID
Primary DI / UDI-DI
00887761000902
Basic UDI-DI
0887761GMN000062UA
Direct marketing DI
00887761000902
FDA product code
IOQ, FNL, OSI
EMDN code
V08060105, V08060106, V08060199
GMDN term
Bariatric bed
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
890.5170, 880.5100
EU registration type
Standard device
EU market of registration
France
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
P7800
GUDID
P7800A
Device classEUDAMED
Class IIa
GUDID
Class II

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Bariatric bed

Similar devices in this category

Other devices filed under ELECTRIC MEDICAL BEDS.

Other devices from Hill-Rom, Inc.

See all devices from Hill-Rom, Inc. →

Properties

  • Serial number
  • Manufacturing date
Other properties (23, all answered No)