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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

125-007 — Class I MDR by Vincent Systems GmbH

MD Atlas
Vincent Systems GmbH

EUDAMED last updated this device on Jun 6, 2025

125-007

426075088emgR8

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Vincent Systems GmbH
UDI-DI code: 04260750880185
Reference / catalog number: 125-007

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Manufacturer information

Organization name: Vincent Systems GmbH
SRN: DE-MF-000016437
Manufacturer status: Active

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128-012426075088accu-monitorYJOn the market 125-023426075088emg-monitorCJOn the market 125-024426075088emg-monitorCJOn the market 125-006426075088emgR8On the market 125-041426075088emgR8On 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 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: 04260750880185
Basic UDI-DI: 426075088emgR8
Reference / catalog number: 125-007
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: Die VINCENTemg dient der Steuerung von myoelektrischen Prothesen der oberen Extremität.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V9015ELECTRODES AND PROBES CUTANEOUS CONDUCTIVE SUBSTANCES

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

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