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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

Ve5-A-BF* — Class I MDR by Vincent Systems GmbH

MD Atlas
Vincent Systems GmbH

EUDAMED last updated this device on Jun 6, 2025

Ve5-A-BF*

426075088evolutionJV

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Vincent Systems GmbH
UDI-DI code: 04260750881748
Reference / catalog number: Ve5-A-BF*

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Manufacturer information

Organization name: Vincent Systems GmbH
SRN: DE-MF-000016437
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: 04260750881748
Basic UDI-DI: 426075088evolutionJV
Reference / catalog number: Ve5-A-BF*
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 VINCENTevolution5 besitzt den medizinischen Zweck der Kompensierung von Verletzungen oder Behinderungen. Dieses Medizinprodukt ist für die exoprothetische und orthoprothetische Versorgung sowie für die Versorgung von Fehlbildungen, Funktionseinschränkungen und Lähmungen der oberen Extremität zu verwenden. Die multiartikulierende Funktionsweise ermöglicht das Greifen, Drücken, Ziehen und Tragen von Gegenständen.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y061803PARTIAL HAND PROSTHESES (INCLUDING FINGERS 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
Serial number
Software identification

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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.