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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

393322 — Class I MDR by FARMAVARI, SAU

MD Atlas
FARMAVARI, SAU

EUDAMED last updated this device on Jun 26, 2025

393322

8431479C143W3

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: FARMAVARI, SAU
UDI-DI code: 08431479933223
Reference / catalog number: 393322

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Manufacturer information

Organization name: FARMAVARI, SAU
SRN: ES-MF-000011556
Manufacturer status: Active

Critical warnings

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

CW262
EUDAMED did not publish a description for this code.
CW999
Hipersensibilidad a los tejidos.

Market distribution

Primary placement in Spain; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 08431479933223
Basic UDI-DI: 8431479C143W3
Reference / catalog number: 393322
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: Indicadas para la prevención, tratamiento y alivio de varices y otras patologías vasculares. Trastornos venosos moderados, telangiectasias (arañas vasculares) o venas reticulares. Piernas cansadas con síntomas de pesadez, hinchazón, calambres, tobillos hinchados, etc. Acción relajante y descanso para las piernas. Conformes a la clasificación CEAP 0 y 1.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M030405COMPRESSION STOCKINGS

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

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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.