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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

0021205 — Class I MDR by LIDERMED S.A.

MD Atlas
LIDERMED S.A.

EUDAMED last updated this device on Apr 9, 2026

0021205

18426716LGRIP01QQ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LIDERMED S.A.
UDI-DI code: 08426716212056
Reference / catalog number: 0021205

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Manufacturer information

Organization name: LIDERMED S.A.
SRN: ES-MF-000004664
Manufacturer status: Active

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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.

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08426716212056
Basic UDI-DI: 18426716LGRIP01QQ
Reference / catalog number: 0021205
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: Medias anti-embólicas con orificio de inspección para la verificación de la circulación sanguínea. Ayudan a prevenir la formación de coágulos sanguíneos en las extremidades inferiores, particularmente en pacientes que tienen un riesgo aumentado de embolia o trombosis venosa profunda.
Additional information URL: https://www.lidermed.com/
Clinical sizes: 1 MU999

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

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Expiration date
Manufacturing date
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Software identification