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.

Medilon Genustab Kniebrace — 9 UDI-DI variants, MDR (Medilon Braces)

MD Atlas
Medilon Braces

Data from EUDAMED, last updated May 30, 2026

Medilon Genustab Kniebrace

8720865045KNB-STABZH

9 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: Medilon Braces

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: 8720865045KNB-STABZH
Device name: —
Device model: Medilon Genustab Kniebrace
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 29, 2025

Manufacturer & authorised representative

Manufacturer

Name: Medilon Braces
SRN: NL-MF-000047759
Country: Netherlands
Email: medilonbraces@gmail.com
Phone: 0631171964

Variants by status

UDI-DI variants

9 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

basicUdiUlid01JWDZJHWAVZB20Y1NS917E859

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

MB700408720865045061
MB700408720865045108
MB700408720865045320
MB700408720865045078
MB7004-208720865045436
MB7004-208720865045467
MB700408720865045092
MB7004-208720865045443
MB700408720865045085