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Lenosoft S

EUDAMED

Class I (EU MDR)

Ref 13232

by FARMABAN s.a.

Identity

Trade Name
LENOSOFT S EUDAMED
Device Name
LENOSOFT EUDAMED
Model / Reference
13232 EUDAMED

Identifiers

Primary DI / UDI-DI
08428012032321 EUDAMED
Basic UDI-DI
8428012GUATAWL EUDAMED
EMDN Code
M030102 NON-WOVEN BANDAGES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Lenosoft S by FARMABAN s.a. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
FARMABAN s.a.
EUDAMED SRN
ES-MF-000004713

Sources (1)

  • EUDAMED 78f26f9c-e8f5-46fd-a960-4723a245e5b8 61 fields · synced Jun 18, 2026