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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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NordBed™ Ultra — 43 UDI-DI variants, MDR (Invacare Rea AB)

MD Atlas
Invacare Rea AB

Data from EUDAMED, last updated May 31, 2026

NordBed™ Ultra

7331226NordbedUltraKE

43 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Invacare Rea AB

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 7331226NordbedUltraKE
Device name: NordBed™ Ultra
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 18, 2025

Manufacturer & authorised representative

Manufacturer

Name: Invacare Rea AB
SRN: SE-MF-000003772
Country: Sweden
Email: Compliance_Sweden@invacare.com

Variants by status

UDI-DI variants

43 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KCRMS488Q2E38K1DGVBQNJ1Y

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

1654219_S107323410162261
1651528_S107323410156772
1657669_S107323410167921
165766907323410167914
165526307323410163398
165080407323410153900
1649919_S107323410152880
1649885_S307323410156918
165571307323410164623
1655263_S107323410163404
1650272_S107323410153115
1660805_S107323410175858
1649660_S507323410152910
165030007323410153139
1649926_S107323410153375
1649660_S307323410152323
164988507323410152248
1649923_S107323410167549

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