OSYPKA GmbH

Germany DE-MF-000005610 Last updated 23 Oct 2026

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Devices: 28
Registries: EUDAMEDFDA
FDA recalls: 0

Catalogue28

VACS II 18.0 x 40 Ref YA0044

Class III EUDAMED Active
VACS III 20.0 x 40 Ref YA32040

Class III EUDAMED Active
VACS III 22.0 x 60 Ref YA32260

Class III EUDAMED Active
VACS II 18.0 x 60 Ref YA0046

Class III EUDAMED Active
VACS II 26.0 x 30 Ref YA0058

Class III EUDAMED Active
VACS III 18.0 x 30 Ref YA31830

Class III EUDAMED Active
VACS II 16.0 x 50 Ref YA0037

Class III EUDAMED Active
Pk-143-B Ref 460041

Class I EUDAMED Active
Cable D2-SP |blue|L=2500| Ref 81973

Class I EUDAMED Active
Cable D2P-SP |white|L=2500| Ref 81986WS

Class I EUDAMED Active
CELSIUS - iCONNECT Ref 001-009071-1

Class I EUDAMED Active
VACS II 12.0 x 60 Ref YA0026

Class III EUDAMED Active
VACS II 12.0 x 20 Ref YA0023

Class III EUDAMED Active
VACS II 12.0 x 40 Ref YA0025

Class III EUDAMED Active
CX-BSW-Abbott Ref 82017

Class I EUDAMED Active

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?

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
LinkedIn: linkedin.com/company/osypka-ag/mycompany
Facebook: facebook.com/profile.php
Email: [email protected]
Phone: +49 7623 7405 0
PRRC contact: Achim Kitschmann
EUDAMED SRN: DE-MF-000005610
FDA FEI number: 3003923762
DUNS number: 316276799

Catalogue28

VACS II 18.0 x 40 Ref YA0044

VACS III 20.0 x 40 Ref YA32040

VACS III 22.0 x 60 Ref YA32260

VACS II 18.0 x 60 Ref YA0046

VACS II 26.0 x 30 Ref YA0058

VACS III 18.0 x 30 Ref YA31830

VACS II 16.0 x 50 Ref YA0037

Pk-143-B Ref 460041

Cable D2-SP |blue|L=2500| Ref 81973

Cable D2P-SP |white|L=2500| Ref 81986WS

CELSIUS - iCONNECT Ref 001-009071-1

VACS II 12.0 x 60 Ref YA0026

VACS II 12.0 x 20 Ref YA0023

VACS II 12.0 x 40 Ref YA0025

CX-BSW-Abbott Ref 82017

About

What OSYPKA GmbH makes

Frequently asked questions

Information