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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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Actimo Liberty — 2 UDI-DI variants, MDR (Rehaforum Medical GmbH)

MD Atlas
Rehaforum Medical GmbH

Data from EUDAMED, last updated May 23, 2026

Actimo Liberty

4041314actimoliberty2Q

2 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: Rehaforum Medical GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4041314actimoliberty2Q
Device name: Actimo Liberty
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 18, 2025

Manufacturer & authorised representative

Manufacturer

Name: Rehaforum Medical GmbH
SRN: DE-MF-000018288
Country: Germany
Email: info@rehaforum.com
Phone: +49 4121 473312

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01K0ENBJ4HFRZ7WCX0E1ZEHN9T

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

8009484304041314041392
8009484204041314041385