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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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Octave® — 9 UDI-DI variants, MDR (Invacare Rea AB)

MD Atlas
Invacare Rea AB

Data from EUDAMED, last updated May 31, 2026

Octave®

7331226OctaveJ5

9 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: 7331226OctaveJ5
Device name: Octave®
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

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KCRMWDE8SRFE2DS5JZADEH81

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

OCTAVE.A2EB1.M107323410100010
OCTAVE_A3EB1_M1_107323410133476
OCTAVE-C2AB1-M107323410099994
OCTAVE_C2AB1_M1_107323410100058
OCTAVE.A1EB1.M107323410100003
155508807323410054559
OCTAVE.C2UB1.M107323410100034
OCTAVE.C1AB1.M107323410100027
OCTAVE_A2EB1_M1_107323410100041