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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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Rehabilitation Set — 5 UDI-DI variants, MDR

MD Atlas
Novafon Elektromedizinische Geräte GmbH

Data from EUDAMED, last updated May 23, 2026

Rehabilitation Set

426020379RehaF9

5 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: Novafon Elektromedizinische Geräte GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426020379RehaF9
Device name: Rehabilitation Set
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 7, 2022

Manufacturer & authorised representative

Manufacturer

Name: Novafon Elektromedizinische Geräte GmbH
SRN: DE-MF-000006137
Country: Germany
Email: info@novafon.de
Phone: 00497151133970

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01FYY57AH2TTQJ31DSMW9BMTC2

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

Reha Set one | black04260203793406
Reha Set one | white04260203793390
Rehabilitation Set black04260203792409
703604260203791655
701604260203791181