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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

BIOCONTACT FORMS — Class I MDR by Laboratoire Atoutbio

MD Atlas
Laboratoire Atoutbio

EUDAMED last updated this device on Apr 15, 2026

BIOCONTACT FORMS

3770042459BIOCONTACTF2L

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Laboratoire Atoutbio
UDI-DI code: 03770042459001
Reference / catalog number: BIOCONTACT FORMS

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Manufacturer information

Organization name: Laboratoire Atoutbio
SRN: FR-MF-000053049
Manufacturer status: Active

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: 03770042459001
Basic UDI-DI: 3770042459BIOCONTACTF2L
Reference / catalog number: BIOCONTACT FORMS
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: Création et gestion de formulaires pour permettre aux utilisateurs d'obtenir un retour d'information/résultat personnel en fonction de leurs informations rentrées.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V92MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES

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

Related devices

This device is not currently linked to any other device.

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.