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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Alternating-pressure bed mattress — 3 UDI-DI variants, MDR

MD Atlas
Hill-Rom S.A.S.

Data from EUDAMED, last updated May 19, 2026

Alternating-pressure bed mattress

0887761GMN000090UF

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Hill-Rom S.A.S.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 0887761GMN000090UF
Device name: Alternating-pressure bed mattress
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 18, 2025

Manufacturer & authorised representative

Manufacturer

Name: Hill-Rom S.A.S.
SRN: FR-MF-000003176
Country: France
Email: HRC_Global_Adverse_Event_Reporting@baxter.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KACF0CEWPWWJS2THR26EEPW6

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Baxter00887761977556
Baxter00887761977594
Baxter00887761977532