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 BRILLANT II.KT -… — 280 UDI-DI variants, MDR

MD Atlas
MAXIS a.s.

Data from EUDAMED, last updated May 23, 2026

Kompresní punčochy BRILLANT II.KT - Stehenní punčocha s krajkou

8591285AGKB2YV

280 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: 8591285AGKB2YV
Device name: Kompresní punčochy BRILLANT II.KT - Stehenní punčocha s krajkou
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 23, 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

280 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

basicUdiUlid01KPWEFZT0Z2MZJ7VPZCJD08VD

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

859128582631408591285826314
859128582632108591285826321
859128505952108591285059521
859128582643708591285826437
859128582641308591285826413
859128582642008591285826420
859128505919408591285059194
859128582153108591285821531
859128509870408591285098704
859128582151708591285821517
859128582152408591285821524
859128505920008591285059200
859128582163008591285821630
859128509871108591285098711
859128582161608591285821616
859128582162308591285821623
859128505955208591285059552
859128582663508591285826635
859128582661108591285826611
859128582662808591285826628
859128505956908591285059569
859128582673408591285826734
859128582671008591285826710
859128582672708591285826727
859128505923108591285059231