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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

VA12X — Class I MDR by ORTHOSOFT

MD Atlas
ORTHOSOFT

EUDAMED last updated this device on Mar 4, 2025

VA12X

37602703434010774527A

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ORTHOSOFT
UDI-DI code: 03760270340011
Reference / catalog number: VA12X

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Manufacturer information

Organization name: ORTHOSOFT
SRN: FR-MF-000000216
Manufacturer status: Active

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CA11X37602703434010484836TOn the market CA12X37602703434010484836TOn the market CU11X37602703434010484846VOn the market EP11X3760270343401077455BOn the market FL12D37602703434010449376HOn the market

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.

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: not provided
UDI-DI code: 03760270340011
Basic UDI-DI: 37602703434010774527A
Reference / catalog number: VA12X
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y062403FOOT PARTIAL PROSTHESES (INCLUDING TOE PROSTHESES)

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
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Software identification