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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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Alpha — 12 UDI-DI variants, MDR (Invacare Rea AB)

MD Atlas
Invacare Rea AB

Data from EUDAMED, last updated May 31, 2026

Alpha

7331226Alpha7B

12 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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7331226Alpha7B
Device name: Alpha
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

12 UDI-DI variants

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Applied filters

basicUdiUlid01KCRJHYZ4VS8JAXQ5XD6QFW03

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

12220-35-21L07331492065066
12220-35-2107331492062959
12220-02-35-2107331492005925
1510628-00107331492568840
12230-35-2107331492062997
12230-35-21L07331492065059
12230-35-2707331492063000
12230-02-35-2107331492005956
12230-35-21R07331492065110
12230-35-2407331492063185
12230-35-8707331492063116
12230-02-35-2307331492560240