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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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Kit « Mon suivi Ortho » taille enfant — 3 UDI-DI variants, MDR

MD Atlas
innOralis

Data from EUDAMED, last updated May 19, 2026

Kit « Mon suivi Ortho » taille enfant

377002411409_310BV

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: innOralis

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 377002411409_310BV
Device name: Kit « Mon suivi Ortho » taille enfant
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 29, 2023

Manufacturer & authorised representative

Manufacturer

Name: innOralis
SRN: FR-MF-000010971
Country: France
Email: contact@innoralis.fr
Phone: +33384558992

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01HBGRV5JJ0JP4B2RPSJR37W29

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

09_310_1003770024114508
09_31003770024114492
09_310_4003770024114621