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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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VMS2 — 4 UDI-DI variants, MDR (Valmy Industries SAS)

MD Atlas
Valmy Industries SAS

Data from EUDAMED, last updated May 19, 2026

VMS2

3700603VMS2-XXETB

4 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: Valmy Industries SAS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3700603VMS2-XXETB
Device name: VMS2
Device model: Masque à usage médical - Type II - SURGEOR
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 7, 2025

Manufacturer & authorised representative

Manufacturer

Name: Valmy Industries SAS
SRN: FR-MF-000010356
Country: France
Email: laurent.suissa@segetex.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01J2TN3EJ63KFJQ9350ZZFFBW4

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

VMS2-0103700603053683
VMS2-0303700603053706
VMS2-05C4003700603053720
VMS2-0703700603053119