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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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Futura™ — 60 UDI-DI variants, MDR (Invacare Rea AB)

MD Atlas
Invacare Rea AB

Data from EUDAMED, last updated May 31, 2026

Futura™

7331226FuturaP6

60 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: 7331226FuturaP6
Device name: Futura™
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

60 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KCRK0WV2AN65XW9GHQPQ27R5

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

12076-43-21L07331492561032
12076-43-2707331492561087
12076-43-21CBL07331492564668
12076-43-27CBR07331492564699
12076-43-2307331492561056
166065107331492597505
12076-43-27CBL07331492564682
12083-43-0107331492562190
12076-43-2107331492560745
12076-43-21CBR07331492564675

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