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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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Skarpetki zdrowotne profilaktyczne — 8 UDI-DI variants, MDR

MD Atlas
JJW Spółka Jawna J. Karpiński, J. Rudnicki, W. Lewin

Data from EUDAMED, last updated May 30, 2026

Skarpetki zdrowotne profilaktyczne

5901050MedicDeoMaxFlexV2

8 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: JJW Spółka Jawna J. Karpiński, J. Rudnicki, W. Lewin

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5901050MedicDeoMaxFlexV2
Device name: Skarpetki zdrowotne profilaktyczne
Device model: Medic Deo MaxFlex
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 10, 2024

Manufacturer & authorised representative

Manufacturer

Name: JJW Spółka Jawna J. Karpiński, J. Rudnicki, W. Lewin
SRN: PL-MF-000009541
Country: Poland
Email: info@jjw.pl
Phone: +48 22 711 71 58

Variants by status

UDI-DI variants

8 UDI-DI variants

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basicUdiUlid01HKSW1NDVR9C9CVAMN0JE5HS1

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

MDM05901050302739
MDM05901050302630
MDM05901050502788
MDM05901050302838
Medic Deo MaxFlex05901050502887
MDM05901050502689
MDM05901050502580
MDM05901050302531