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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

SO1006 — Class I MDR by FARMABAN s.a.

MD Atlas
FARMABAN s.a.

EUDAMED last updated this device on Jul 31, 2025

SO1006

8428012VF503-201AS

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: FARMABAN s.a.
UDI-DI code: 08428012302806
Reference / catalog number: SO1006

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Manufacturer information

Organization name: FARMABAN s.a.
SRN: ES-MF-000004713
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.

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW999
CONTRE-INDICATIONS Ne pas utiliser en cas de problèmes artériels, de graves problèmes vasculaires et en cas d'oedème sévère (sur avis médical). Hypersensibilité à un des constituants PRECAUTIONS D'EMPLOI Atteintes graves nécessitant une immobilisation totale. Appliquer sur peau propre et sèche. Ne pas appliquer en cas de fragilité cutanée ou directment sur une plaie cutanée. Ne jamais appliquer la bande en tension maximale. En cas d'engourdissements ou de sensations douloureses, ôtez la bande et refaites le bandage moins serré. Si la douleur persiste ou en cas de difficultés, demandez conseil a votre pharmacien, kinésithérapeute ou à votre médecin.
CW009
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08428012302806
Basic UDI-DI: 8428012VF503-201AS
Reference / catalog number: SO1006
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: Bande adhésive élastique hypoallergénique
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 2.5 MU36
6 MU10

EMDN nomenclature code(s)

M03040199ELASTIC COMPRESSION BANDAGES - 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