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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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Adjonction pour cale d'abduction — 5 UDI-DI variants, MDR

MD Atlas
JANTON (G2M)

Data from EUDAMED, last updated May 19, 2026

Adjonction pour cale d'abduction

3666322POSADCAL8Z

5 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: 3666322POSADCAL8Z
Device name: —
Device model: Adjonction pour cale d'abduction
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 24, 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

5 UDI-DI variants

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Applied filters

basicUdiUlid01G6A5RPH8X835ZX2YDKJB87R5

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

Mechanical abduction wedge system03666322301125
Mechanical system wedge adbuction03666322301118
NOTCHED ABDUCTION WEDGE03666322301514
NOTCHED ABDUCTION WEDGE03666322301507
Removable abduction wedge03666322301132