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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

méditech — Class I MDR by FARMABAN s.a.

MD Atlas
FARMABAN s.a.

EUDAMED last updated this device on Nov 18, 2024

méditech

8428012VEAN104QJ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: FARMABAN s.a.
UDI-DI code: 08428012302615
Reference / catalog number: SO1003

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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

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

CW083
EUDAMED did not publish a description for this code.
CW999
Atteintes graves nécessitant une immobilisation totale. Appliquer dur peau et sèche. Ne pas appliquer en cas de fragilité cutanée ou directeent sur une plaie cutanée. Ne jamais appliquer la bande en tension maximale. En cas d'engourdissements ou de sensations douloureuses, ôtez la bande et refaites le bandage moins serre. Si la douleur persiste ou en cas de difficultés, demandez conseil a votre pharmacien, kinésithérapeute ou à votre médecin.
CW999
Ne pas utiliser en cas de problèmes artériels, de graves problèmes vasculaires et en cas d'oedème sévère (sur avis médical).

Market distribution

Primary placement in France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: méditech
UDI-DI code: 08428012302615
Basic UDI-DI: 8428012VEAN104QJ
Reference / catalog number: SO1003
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: Support tissé 100% coton, masse adhésive hypoallergénique sans latex. Bande à fort pouvoir adhésif et permeable à l'air.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 2.5 MU10
4.5 MU36

EMDN nomenclature code(s)

M03040199ELASTIC COMPRESSION BANDAGES - OTHER
M03030199ELASTIC FIXING BANDAGES - OTHER
M03040299ELASTIC SUPPORT 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