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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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Articulations de genou — 3 UDI-DI variants, MDR (JANTON (G2M))

MD Atlas
JANTON (G2M)

Data from EUDAMED, last updated May 19, 2026

Articulations de genou

3666322ORTAGENOUS4

3 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: JANTON (G2M)

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3666322ORTAGENOUS4
Device name: —
Device model: Articulations de genou
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 1, 2022

Manufacturer & authorised representative

Manufacturer

Name: JANTON (G2M)
SRN: FR-MF-000003877
Country: France
Email: info@janton-solutions.com
Phone: 0241500399

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01G9CVDWS8EJE4YJA0738W9R61

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

EXTERNAL LEFT OMEGA KNEE JOINT03666322203559
EXTERNAL RIGHT OMEGA KNEE JOINT03666322203542
Hoffa locked joint 18x403666322201166