Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

0021201 — Class I MDR by LIDERMED S.A.

MD Atlas
LIDERMED S.A.

EUDAMED last updated this device on Apr 9, 2026

0021201

18426716LGRIP01QQ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LIDERMED S.A.
UDI-DI code: 08426716212018
Reference / catalog number: 0021201

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

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

Related devices

011015418426716ALIVI01KKOn the market 011015118426716ALIVI01KKOn the market 011015218426716ALIVI01KKOn the market 011014518426716ALIVI01KKOn the market 011015518426716ALIVI01KKOn 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.

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: 08426716212018
Basic UDI-DI: 18426716LGRIP01QQ
Reference / catalog number: 0021201
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 MU161

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