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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 -… — 181 UDI-DI variants, MDR

MD Atlas
MAXIS a.s.

Data from EUDAMED, last updated May 23, 2026

Kompresní punčochy MICRO I.KT - Punčochové kalhoty

8591285ATM18C

181 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

181 UDI-DI variants

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Applied filters

basicUdiUlid01KPQ736CXBP26GPMGRVVNV3GS

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

859128507803408591285078034
859128587283008591285872830
859128587285408591285872854
859128587281608591285872816
859128587282308591285872823
859128507804108591285078041
859128587288508591285872885
859128587290808591285872908
859128587286108591285872861
859128587287808591285872878
859128507805808591285078058
859128514985708591285149857
859128587293908591285872939
859128512528808591285125288
859128587295308591285872953
859128587291508591285872915
859128587292208591285872922
859128507806508591285078065
859128514726608591285147266
859128587298408591285872984
859128587300408591285873004
859128587296008591285872960
859128587297708591285872977
859128514967308591285149673
859128507807208591285078072

1 2 3 4 5

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8591285ATM18C
Device name: Kompresní punčochy MICRO I.KT - Punčochové kalhoty
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