Skip to content

Pannoc Chemie

Belgium BE-MF-000004682 Last updated 21 Oct 2026

Devices
2
Registries
EUDAMED
FDA recalls
0

Catalogue2

  • Rodilan Ref many

    Class I EUDAMED Active
  • Rodisonic Ref many

    Class I EUDAMED Active

About

At Pannoc we guide you from concept to end product. Thanks to our expertise in development, production and quality control, we offer flexible solutions.

Translated from the manufacturer's own website. Source

What Pannoc Chemie makes

Pannoc Chemie manufactures Rodilan and Rodisonic, which are classified as Class I medical devices. These products appear to include pharmaceutical or chemical formulations intended for medical use, though specific applications are not detailed.

The company’s devices are listed in the EU’s eudamed registry under Class I classification. Pannoc Chemie is based in Belgium.

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

Frequently asked questions

What types of medical devices does Pannoc Chemie manufacture?

Pannoc Chemie manufactures Rodilan and Rodisonic, which are classified as Class I medical devices. These devices appear to be pharmaceutical or chemical formulations intended for medical applications, though their exact uses are not specified in the available data.

Where is Pannoc Chemie based?

Pannoc Chemie is based in Belgium. The company’s location is relevant for regulatory compliance, particularly when considering EU-specific requirements for medical devices.

Are Pannoc Chemie’s devices listed in any regulatory registries?

Yes, Pannoc Chemie’s devices are listed in the EU’s eudamed registry. This registry is used for transparency in the European medical device market, allowing stakeholders to verify the existence and classification of devices.

How are Pannoc Chemie’s devices classified under EU regulations?

Pannoc Chemie’s devices, including Rodilan and Rodisonic, are classified as Class I medical devices. This classification is determined by factors such as the risk associated with the device’s use, and Class I typically represents the lowest risk category in the EU’s medical device regulatory framework.

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

Information

Country
Belgium
Address
23, Lammerdries-Oost, Olen, Belgium
Website
www.pannoc.eu
Phone
+3214217018
PRRC contact
Roel Jacobs
EUDAMED SRN
BE-MF-000004682