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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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Organization name
UDI-DI code
Reference / catalog number

VMS2-03 — Class I MDR by Valmy Industries SAS

MD Atlas
Valmy Industries SAS

EUDAMED last updated this device on Jun 19, 2025

VMS2-03

3700603VMS2-XXETB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Valmy Industries SAS
UDI-DI code: 03700603053706
Reference / catalog number: VMS2-03

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Manufacturer information

Organization name: Valmy Industries SAS
SRN: FR-MF-000010356
Manufacturer status: Active

Critical warnings

3 warnings recorded — scroll inside the panel to see all entries.

CW009
EUDAMED did not publish a description for this code.
CW032
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: VMS2-03
UDI-DI code: 03700603053706
Basic UDI-DI: 3700603VMS2-XXETB
Reference / catalog number: VMS2-03
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 50
Additional product description: Ce masque à usage médical adulte est destiné à protéger l’environnement et l’entourage du patient qui porte ce masque des risques de contamination bactérienne (gouttelettes émises lors de la toux, des éternuements et de la parole).
Additional information URL: https://www.valmy.eu/wp-content/uploads/2025/03/NOTICE-MASQ-CHIR-II-V1.pdf
Clinical sizes: Bleu

EMDN nomenclature code(s)

T020604MEDICAL USE FACE MASKS, TYPE II AND IIR

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

VMS2-013700603VMS2-XXETBOn the market VMS2-02C203700603VMS2-XXLTROn the market VMS2-04C203700603VMS2-XXLTROn the market VMS2-05C403700603VMS2-XXETBOn the market VMS2-073700603VMS2-XXETBOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.