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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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mobee® flex — 1 UDI-DI variant, MDR (SportMed S.A.)

MD Atlas
SportMed S.A.

Data from EUDAMED, last updated Jun 2, 2026

mobee® flex

426246573MFX1C9

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: SportMed S.A.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426246573MFX1C9
Device name: mobee® flex
Device model: MFX
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 1, 2026

Manufacturer & authorised representative

Manufacturer

Name: SportMed S.A.
SRN: LU-MF-000040759
Country: Luxembourg
Email: info@mobee.eu
Phone: +352 2672 0101

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KT1MTAKBQ802G8TT8PD6ZWD5

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

mobee® flex04262465730014