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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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Orca — 26 UDI-DI variants, MDR (Invacare GmbH)

MD Atlas
Invacare GmbH

Data from EUDAMED, last updated May 23, 2026

Orca

4028698OrcaDT

26 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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UDI-DI variants

26 UDI-DI variants

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Applied filters

basicUdiUlid01KCPDR4KR8B6RXW2JC798P3P4

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

Orca04028698125313
Orca04028698125603
Orca04028698125269
Orca04028698125252
Orca04028698125320
Orca04028698125634
Orca04028698125207
Orca04028698125283
Orca04028698125474
Orca04028698125047
Orca04028698125245
Orca04028698125412
Orca04028698125559
Orca04028698125580
Orca04028698125191
Orca04028698125627
Orca04028698125238
Orca04028698125368
Orca04028698125344
Orca04028698125566
Orca04028698125573
Orca04028698125184
Orca04028698125214
Orca04028698125290
Orca04028698125276

1 2

Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4028698OrcaDT
Device name: Orca
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 17, 2025

Manufacturer & authorised representative

Manufacturer

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

Variants by status