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

MD Atlas
Invacare GmbH

Data from EUDAMED, last updated May 23, 2026

Ocean VIP Ergo

4028698OceanVIPErgoRR

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: 4028698OceanVIPErgoRR
Device name: Ocean VIP 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

basicUdiUlid01KEVSDB6BPYNKTFMT6AV80WVW

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 Dual VIP Ergo04028698132656
Ocean Dual VIP Ergo04028698132663
Ocean Dual VIP Ergo04028698133288
Ocean Dual VIP Ergo04028698133837
Ocean Dual VIP Ergo04028698133295
Ocean VIP Ergo04028698133820
Ocean VIP Ergo04028698133271
Ocean VIP Ergo04028698133264
Ocean VIP Ergo04028698132618
Ocean VIP Ergo04028698132625