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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™ Optimo — 92 UDI-DI variants, MDR (Invacare Rea AB)

MD Atlas
Invacare Rea AB

Data from EUDAMED, last updated May 31, 2026

NordBed™ Optimo

7331226NordbedOptimoGE

92 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: 7331226NordbedOptimoGE
Device name: NordBed™ Optimo
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

92 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KCRMNJQCT5SHNNF5SMPX4R2E

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

1649849_S107323410151142
166078407323410175001
165526407323410163411
1660656_S107323410170594
166065607323410170587
1649849_S207323410175483
1653920_S107323410160243
165699107323410167488
1655715_S107323410164678
1654218_S207323410175100
165526507323410163435
1660656_S207323410170686
1659820_S107323410168720
164984707323410151128
1654218_S107323410162193
1655264_S107323410163428
165392007323410160236

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