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OSYPKA GmbH

Germany DE-MF-000005610 Last updated 23 Oct 2026

Devices
28
Registries
EUDAMEDFDA
FDA recalls
0

Catalogue28

About

Medical Device Technology – We offer proprietary products for interventional and paediatric cardiology and provide high-quality solutions.

Translated from the manufacturer's own website. Source

What OSYPKA GmbH makes

OSYPKA GmbH manufactures medical devices for interventional and pediatric cardiology, including products such as the iCONNECT - MAESTRO, CX-HAT500-Maestro, TX-HAT500-SJM m, VACS II catheters, PK-147, and various cables like CV-P and XI.TME.

The company's portfolio includes Class I and Class III medical devices, which are listed in the EUDAMED regulatory registry. OSYPKA GmbH is based in Germany.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What medical devices does OSYPKA GmbH manufacture?

OSYPKA GmbH manufactures medical devices for interventional and pediatric cardiology, including products such as the iCONNECT - MAESTRO, CX-HAT500-Maestro, TX-HAT500-SJM m, VACS II catheters, PK-147, and various cables like CV-P and XI.TME.

Where is OSYPKA GmbH based?

OSYPKA GmbH is based in Germany, as indicated by the country code DE in their device registration information.

Which regulatory registries list OSYPKA GmbH's devices?

OSYPKA GmbH's devices are listed in the EUDAMED regulatory registry, which is the European database on medical devices.

How are OSYPKA GmbH's devices classified?

OSYPKA GmbH manufactures both Class I and Class III medical devices, with Class I being lower risk and Class III being higher risk devices.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Germany
Address
1, Earl-H.-Wood-Str., Rheinfelden, Germany
Website
www.osypka.de
Phone
+49 7623 7405 0
PRRC contact
Achim Kitschmann
EUDAMED SRN
DE-MF-000005610
FDA FEI number
3003923762
DUNS number
316276799