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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

M 015 — Class I MDR by MARTÍN VECINO, S.L.

MD Atlas
MARTÍN VECINO, S.L.

EUDAMED last updated this device on Dec 30, 2025

M 015

84354071ARNESVMY

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MARTÍN VECINO, S.L.
UDI-DI code: 18435407102108
Reference / catalog number: M 015

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Manufacturer information

Organization name: MARTÍN VECINO, S.L.
SRN: ES-MF-000013754
Manufacturer status: Active

Market distribution

Primary placement in Spain; available across 2 countries total.

Country	On market since	Until
SpainPrimary placement		Still on market
Portugal		Still on market

Device identification

Trade name: not provided
UDI-DI code: 18435407102108
Basic UDI-DI: 84354071ARNESVMY
Reference / catalog number: M 015
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: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

R9099RESPIRATORY AND ANAESTHESIA DEVICES - OTHER

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

M 07284354071ARNESGM2On the market M 07384354071ARNESGM2On the market M 08784354071ARNESGM2On the market M 06284354071ARNESGM2On the market M 16484354071ARNESGM2On 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.