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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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GEMINI CHUT à Décharge de l'avant du… — 84 UDI-DI variants, MDR

MD Atlas
IMPLANTS SERVICE ORTHOPEDIE

Data from EUDAMED, last updated May 19, 2026

GEMINI CHUT à Décharge de l'avant du pied

3615570GEMINIR2

84 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: IMPLANTS SERVICE ORTHOPEDIE

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3615570GEMINIR2
Device name: GEMINI CHUT à Décharge de l'avant du pied
Device model: GEMINI
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 30, 2021

Manufacturer & authorised representative

Manufacturer

Name: IMPLANTS SERVICE ORTHOPEDIE
SRN: FR-MF-000000297
Country: France
Email: durier@evolutis-group.com
Phone: +33169021920

Variants by status

UDI-DI variants

84 UDI-DI variants

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Applied filters

basicUdiUlid01FQXQA51RX3JC2HX0R80PY7V8

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

GEMINI TAILLE 4203615570000083
GEMINI TAILLE 4303615570000120
GEMINI TAILLE 4403615570000137
GEMINI TAILLE 4503615570000144
GEMINI TAILLE 4603615570000151
GEMINI TAILLE 4703615570000465
GEMINI TAILLE 4803615570000472
GEMINI TAILLE 4903615570000489
GEMINI TAILLE 5003615570000496

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