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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 PROMAX Standard… — 128 UDI-DI variants, MDR

MD Atlas
MAXIS a.s.

Data from EUDAMED, last updated May 23, 2026

Kompresní punčochy PROMAX Standard I.KT - Stehenní punčocha s neklouzavým zakončením

8591285AGLP12D

128 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

128 UDI-DI variants

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Applied filters

basicUdiUlid01KPYXVH003KG383VJG38YY43M

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

859128528017808591285280178
859128528016108591285280161
859128528019208591285280192
859128528018508591285280185
859128527985108591285279851
859128527984408591285279844
859128527987508591285279875
859128527986808591285279868
859128528021508591285280215
859128528020808591285280208
859128528023908591285280239
859128528022208591285280222
859128527989908591285279899
859128527988208591285279882
859128527991208591285279912
859128527990508591285279905
859128528025308591285280253
859128528024608591285280246
859128528027708591285280277
859128528026008591285280260
859128527993608591285279936
859128527992908591285279929
859128527995008591285279950
859128527994308591285279943
859128528029108591285280291

1 2 3 4 5

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8591285AGLP12D
Device name: Kompresní punčochy PROMAX Standard I.KT - Stehenní punčocha s neklouzavým zakončením
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 24, 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