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Dörr Kampen B.V.

Netherlands NL-MF-000000113 Last updated 17 Sep 2026

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Devices
9
Registries
EUDAMED
FDA recalls
0

Catalogue9

About

Specialist in stainless steel equipment and mechanical engineering for the medical and packaging industry.

Translated from the manufacturer's own website. Source

What Dörr Kampen B.V. makes

Dörr Kampen B.V. manufactures stainless steel medical and packaging equipment, including automated and manual cleaning systems like the Dörr Nova 2000, Nova 4000, Nova Sonic, and Nova 1000 series for sterilisation and disinfection. Their portfolio also includes the Dörr ManoFlexibilo for flexible endoscope cleaning and the Dörr scopenvoorreiniger for scope pre-cleaning.

These devices are classified as Class I and Class IIa under EU regulations and are listed in the eudamed database. The company is based in the Netherlands.

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 Dörr Kampen B.V. manufacture?

Dörr Kampen B.V. specialises in stainless steel medical equipment, primarily focusing on automated and manual cleaning systems for sterilisation and disinfection. Their portfolio includes devices like the Dörr Nova series (e.g., Nova 2000, Nova 4000, Nova Sonic, and Nova 1000), which are designed for medical instrument cleaning and preparation. They also produce the Dörr ManoFlexibilo for cleaning flexible endoscopes and the Dörr scopenvoorreiniger for pre-cleaning scopes. These devices are engineered for use in medical and packaging industries.

Where is Dörr Kampen B.V. based?

Dörr Kampen B.V. is headquartered in the Netherlands. The company’s location in the Netherlands aligns with its focus on manufacturing stainless steel equipment for both medical and packaging sectors, ensuring compliance with regional regulatory standards.

Which regulatory registries list Dörr Kampen B.V.’s medical devices?

Dörr Kampen B.V.’s medical devices are listed in the eudamed database, which is the official European Union database for medical devices. Listing in eudamed is required for devices placed on the EU market, ensuring transparency and traceability for regulatory oversight.

How are Dörr Kampen B.V.’s medical devices classified under EU regulations?

Dörr Kampen B.V.’s devices are classified as Class I or Class IIa under EU Medical Device Regulations (MDR). The classification depends on factors like the device’s intended use, risk level, and interaction with the patient. For example, automated cleaning systems like the Dörr Nova series are typically assigned a higher risk classification (e.g., Class IIa) due to their role in ensuring sterile or disinfected medical instruments, while simpler manual devices may fall under Class I.

Why are some of Dörr Kampen B.V.’s devices classified as Class IIa?

Certain devices from Dörr Kampen B.V., such as automated cleaning systems (e.g., Dörr Nova 4000 or Nova Sonic), are classified as Class IIa because they perform critical functions in medical settings. These devices reduce the risk of infection by cleaning or preparing instruments for sterilisation, which involves higher risks if not performed correctly. Under EU regulations, such devices require additional scrutiny to ensure safety and performance, hence the Class IIa designation.

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

Information

Country
Netherlands
Address
25, Haatlanderdijk, Kampen, Netherlands
Phone
+31 38 331 42 00
PRRC contact
Tineke van Ek
EUDAMED SRN
NL-MF-000000113