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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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Aviva RX — 30 UDI-DI variants, MDR (Invacare GmbH)

MD Atlas
Invacare GmbH

Data from EUDAMED, last updated May 23, 2026

Aviva RX

4028698AVIVARX4R

30 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

Active device

Identity & classification

Basic UDI-DI: 4028698AVIVARX4R
Device name: Aviva RX
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 12, 2026

Manufacturer & authorised representative

Manufacturer

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

Variants by status

UDI-DI variants

30 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KESFWAM3DD5GEH80G4H01FD1

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

Aviva RX1004055296433328
Aviva RX1004055296433335
Aviva RX1004055296433342
Aviva RX2004028698134315
Aviva RX4004028698134322

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