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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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Protège poignet — 2 UDI-DI variants, MDR (NOAO SA)

MD Atlas
NOAO SA

Data from EUDAMED, last updated May 19, 2026

Protège poignet

370176384787800LC

2 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: NOAO SA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 370176384787800LC
Device name: Protège poignet
Device model: Protège poignet
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 24, 2025

Manufacturer & authorised representative

Manufacturer

Name: NOAO SA
SRN: FR-MF-000022232
Country: France
Email: gestioncommerciale@akeo.fr
Phone: +33 02 32 77 27 87

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KD82FE2FSG4A2XYSQ0XW0TXP

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

Protège poignet - Form'Vital - Taille M/L03701763800230
Protège poignet - Form'Vital - Taille S/M03701763800070