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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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Ocean Ergo — 10 UDI-DI variants, MDR (Invacare GmbH)

MD Atlas
Invacare GmbH

Data from EUDAMED, last updated May 23, 2026

Ocean Ergo

4028698OceanErgoC4

10 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 GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4028698OceanErgoC4
Device name: Ocean Ergo
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: Invacare GmbH
SRN: DE-MF-000006985
Country: Germany
Email: compliance@invacare.com

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01KEVSBDG2FEX9HK63AKMWCR94

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

Ocean Ergo04028698132540
Ocean Ergo04028698133196
Ocean Ergo04028698132533
Ocean Ergo04028698133189
Ocean Ergo XL04028698133844
Ocean Ergo XL04028698132564
Ocean Ergo XL04028698132557
Ocean Ergo XL04028698133202
Ocean Ergo XL04028698133219
Ocean Ergo XL04028698133851