Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Kompresní punčochy MICRO II.KT -… — 424 UDI-DI variants, MDR

MD Atlas
MAXIS a.s.

Data from EUDAMED, last updated May 23, 2026

Kompresní punčochy MICRO II.KT - Stehenní punčocha s lemem

8591285AGLM226

424 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.

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8591285AGLM226
Device name: Kompresní punčochy MICRO II.KT - Stehenní punčocha s lemem
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 22, 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

424 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KPSW1SPCTSGEQND022B67JHT

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

859128588518208591285885182
859128588520508591285885205
859128588516808591285885168
859128588517508591285885175
859128506835608591285068356
859128514713608591285147136
859128588528108591285885281
859128588530408591285885304
859128588526708591285885267
859128588527408591285885274
859128506800408591285068004
859128543701508591285437015
859128552738908591285527389
859128508867508591285088675
859128552737208591285527372
859128552735808591285527358
859128552736508591285527365
859128543763308591285437633
859128506801108591285068011
859128552768608591285527686
859128543726808591285437268
859128552767908591285527679
859128552765508591285527655
859128552766208591285527662
859128506838708591285068387