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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… — 192 UDI-DI variants, MDR

MD Atlas
MAXIS a.s.

Data from EUDAMED, last updated May 23, 2026

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

8591285AGLP22F

192 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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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8591285AGLP22F
Device name: Kompresní punčochy PROMAX Standard II.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

UDI-DI variants

192 UDI-DI variants

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Applied filters

basicUdiUlid01KPYXVHSQ4HKZDM6TKHAR2RRE

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

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859128508536008591285085360
859128528265308591285282653

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