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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

0506 — Class I MDR by MEYTEC GmbH…

MD Atlas
MEYTEC GmbH Informationssysteme

EUDAMED last updated this device on May 5, 2026

0506

PP12434TELEDOC82

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MEYTEC GmbH Informationssysteme
UDI-DI code: 13124340506082
Reference / catalog number: 0506

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Manufacturer information

Organization name: MEYTEC GmbH Informationssysteme
SRN: DE-MF-000018939
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 13124340506082
Basic UDI-DI: PP12434TELEDOC82
Reference / catalog number: 0506
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: Der TELEDOC-6 ist als medizinisch elektrisches Gerät für die konsiliarische Tele-Diagnose zwischen vernetzten Standorten (LAN/WLAN und WAN), für die ärztliche Zweitmeinung oder für die Assistenz/ Beratung durch einen nicht vor Ort befindlichen Facharzt zweckbestimmt. Der TELEDOC-6 überträgt und empfängt hierfür Audio- und Video-informationen und ermöglicht darüber hinaus die Bereitstellung weiterer medizinischer Informationen etwa einer fallbasierten Dokumentation und/oder DICOM-Informationen über zentral gehostete Webapplikationen. Zweckbestimmter Anwender ist der medizinische Anwender nach Einweisung und Studium der Gebrauchsanweisung.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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

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.