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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

0110120 — Class I MDR by LIDERMED S.A.

MD Atlas
LIDERMED S.A.

EUDAMED last updated this device on Apr 10, 2026

0110120

18426716ALIVI01KK

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LIDERMED S.A.
UDI-DI code: 08426716101206
Reference / catalog number: 0110120

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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

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: 08426716101206
Basic UDI-DI: 18426716ALIVI01KK
Reference / catalog number: 0110120
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: Aliviovisco® es una tira de espuma de poliuretano flexible, muy transpirable y con efecto viscoelástico que se adapta a la forma del cuerpo distribuyendo el peso de manera uniforme, ofreciendo una óptima posición con una mínima presión sobre el mismo. Se adapta, reconoce y alivia la presión por su alto poder de reparto de presiones. Ideal para la elaboración de plantillas y creación de almohadillados para cualquier parte del cuerpo, ahorrando tiempo del personal médico por su facilidad de uso.
Additional information URL: https://www.lidermed.com/
Clinical sizes: 200 * 10 * 0,5 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

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.