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

0110153 — Class I MDR by LIDERMED S.A.

MD Atlas
LIDERMED S.A.

EUDAMED last updated this device on Apr 13, 2026

0110153

18426716ALIVI01KK

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LIDERMED S.A.
UDI-DI code: 08426716101534
Reference / catalog number: 0110153

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: 08426716101534
Basic UDI-DI: 18426716ALIVI01KK
Reference / catalog number: 0110153
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: Está comprobado que el uso de soportes de fieltro para la descarga de presiones en el pie diabético reduce el tiempo de cicatrización y por consiguiente el riesgo de amputación. Más del 50% de las úlceras plantares tienen su origen en algún tipo de neuropatía (pérdida de sensibilidad). La presión ejercida repetidamente en un mismo punto dispara la probabilidad de desarrollar una úlcera en pacientes diabéticos (con falta de sensibilidad en las extremidades inferiores).
Additional information URL: https://www.lidermed.com/
Clinical sizes: 6 mm x 3 m x 10 cm

EMDN nomenclature code(s)

M040499DRESSINGS FOR WOUNDS, SORES AND ULCERATIONS - 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