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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

S-0051 — Class I MDR by ViALUX Messtechnik +…

MD Atlas
ViALUX Messtechnik + Bildverarbeitung GmbH

EUDAMED last updated this device on Jul 31, 2025

S-0051

PP14208100085

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ViALUX Messtechnik + Bildverarbeitung GmbH
UDI-DI code: 1314208S-0051191
Reference / catalog number: S-0051

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Manufacturer information

Organization name: ViALUX Messtechnik + Bildverarbeitung GmbH
SRN: DE-MF-000006865
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 1314208S-0051191
Basic UDI-DI: PP14208100085
Reference / catalog number: S-0051
Issuing entity: IFA

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: Die BodyLux Messsoftware berechnet aufgrund eines geeigneten, bereitgestellten 3D-Modells Umfangs- und Längenmaße des menschlichen Körpers.
Additional information URL: https://www.bodylux-med.de/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V0399MEASUREMENT DEVICES - 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

Related devices

9714PP14208100085On 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.