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 III.KT -… — 309 UDI-DI variants, MDR

MD Atlas
MAXIS a.s.

Data from EUDAMED, last updated May 23, 2026

Kompresní punčochy MICRO III.KT - Stehenní punčocha s lemem

8591285AGLM328

309 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: 8591285AGLM328
Device name: Kompresní punčochy MICRO III.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

309 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

basicUdiUlid01KPT6RFBN70BAG25ZQP98ANAV

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

859128508130008591285081300
859128590078608591285900786
859128590080908591285900809
859128590076208591285900762
859128590077908591285900779
859128508131708591285081317
859128590088508591285900885
859128590090808591285900908
859128590086108591285900861
859128590087808591285900878
859128508176808591285081768
859128590588008591285905880
859128590590308591285905903
859128590586608591285905866
859128590587308591285905873
859128508177508591285081775
859128590598908591285905989
859128590600908591285906009
859128590596508591285905965
859128590597208591285905972
859128508136208591285081362
859128590108008591285901080
859128590110308591285901103
859128590106608591285901066
859128590107308591285901073

1 2 3 4 5