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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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Kompresní punčochy MICRO I.KT -… — 148 UDI-DI variants, MDR

MD Atlas
MAXIS a.s.

Data from EUDAMED, last updated May 23, 2026

Kompresní punčochy MICRO I.KT - Stehenní punčocha s upínáním v pase levá

8591285UPLM1AX

148 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: MAXIS a.s.

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UDI-DI variants

148 UDI-DI variants

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Applied filters

basicUdiUlid01KPQ7G4T2ZQ9ABTJGY8VVD2B9

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

859128596132908591285961329
859128507792108591285077921
859128587068308591285870683
859128587070608591285870706
859128587066908591285870669
859128587067608591285870676
859128507793808591285077938
859128596139808591285961398
859128596138108591285961381
859128596136708591285961367
859128596137408591285961374
859128507794508591285077945
859128587078208591285870782
859128587080508591285870805
859128587076808591285870768
859128587077508591285870775
859128596144208591285961442
859128596143508591285961435
859128596141108591285961411
859128596142808591285961428
859128587088108591285870881
859128587090408591285870904
859128587086708591285870867
859128587087408591285870874
859128596149708591285961497

2 3 4 5 6

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8591285UPLM1AX
Device name: Kompresní punčochy MICRO I.KT - Stehenní punčocha s upínáním v pase levá
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: MAXIS a.s.
SRN: CZ-MF-000000989
Country: Czechia
Email: info@maxis-medica.com
Phone: +420571633510

Variants by status