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Self-screen B.V.

Netherlands Last updated 8 Jun 2026

Devices
4
Registries
EUDAMED
FDA recalls
0

Catalogue4

About

Self-screen's main focus is on cervical cancer screening and prevention. The company has two clinically validated assays on the market. We strive towards all-molecular screening to ensure objectivity, reproducibility and high-throughput possibilities.

From the manufacturer's own website. Source

What Self-screen B.V. makes

Self-screen B.V. develops an HPV-Risk assay designed for cervical cancer screening, enabling molecular-based risk assessment of human papillomavirus infections.

The HPV-Risk assay is classified under In Vitro Diagnostic (IVD) General and is registered in the EU’s 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

How many devices does Self-screen B.V. have in the registry?

The registry currently lists 4 devices for Self-screen B.V.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Self-screen B.V.'s devices?

Among its 4 most recently registered devices, Self-screen B.V. has devices listed in EUDAMED (4 devices).

What risk classes do Self-screen B.V.'s devices fall under?

Among its 4 most recently registered devices, the classes recorded for Self-screen B.V.'s devices are IVD general. Each device page shows its own class and authorisation.

What are the newest devices from Self-screen B.V. in the registry?

The most recently registered devices listed for Self-screen B.V. include QIAscreen HPV PCR test, QIAsure Methylation Test, PreCursor-M+ and HPV-Risk assay.

Generated automatically from registry data and not verified by a human reviewer.

Information

Address
125, Plesmanlaan, Amsterdam, Netherlands
Phone
+31-850805929
PRRC contact
Albertus Hesselink
EUDAMED SRN
NL-MF-000040204