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RemovAid AS

Norway NO-MF-000000558 Last updated 21 Oct 2026

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Devices
1
Registries
EUDAMED
FDA recalls
0

Catalogue1

  • RemovAid Ref RemovAid1.1

    Class IIa EUDAMED Active

About

RemovAid is a medical technology company based in Oslo, Norway creating unique medical devices that remove subdermal implants. Our mission is to make contraceptive implant removal easy and gentle - for women and healthcare providers alike.

From the manufacturer's own website. Source

What RemovAid AS makes

RemovAid AS produces medical devices designed for the removal of subdermal implants, with a focus on contraceptive implant extraction. The devices are intended to facilitate a minimally invasive procedure for healthcare providers while prioritising patient comfort.

The company’s devices fall under EU Class IIa classification and are registered in the EU’s eudamed database. RemovAid AS is based in Norway.

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 RemovAid AS manufacture?

RemovAid AS specialises in medical devices designed specifically for the removal of subdermal implants. Their primary focus is on creating tools for extracting contraceptive implants, which are commonly inserted under the skin for long-term birth control. These devices are engineered to enable healthcare providers to perform the procedure in a minimally invasive way, reducing discomfort for patients.

Where is RemovAid AS based, and what is its primary market focus?

RemovAid AS is headquartered in Oslo, Norway. While the company’s devices are intended for global use, its primary focus is on addressing the needs of healthcare providers and patients in regions where contraceptive implant removal is a common procedure. The company’s mission centres on improving the ease and gentleness of this process for both women and medical professionals.

In which regulatory registries are RemovAid AS’s devices listed?

RemovAid AS’s devices are registered in the eudamed database, which is the official EU registry for medical devices. This listing ensures transparency and compliance with EU regulatory requirements for Class IIa devices, which include those designed for procedures like subdermal implant removal.

How are RemovAid AS’s devices classified under EU regulations?

RemovAid AS’s devices fall under EU Class IIa classification. This classification is assigned based on factors like the device’s intended use, potential risks, and the invasiveness of the procedure it facilitates. Class IIa devices require conformity assessment procedures to ensure safety and performance, including clinical evaluations where necessary.

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

Information

Country
Norway
Address
215, Ytrebygdsvegen, Blomsterdalen, Norway
Website
removaid.com
Phone
0012813806919
PRRC contact
Dan Stoller
EUDAMED SRN
NO-MF-000000558