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inmutouch.com ApS

Denmark DK-MF-000020064 Last updated 17 Sep 2026

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Devices
4
Registries
EUDAMED
FDA recalls
0

Catalogue4

  • inmuJOY Ref 5744000890159

    Class I EUDAMED Active
  • inmuRELAX Ref 5744000890142

    Class I EUDAMED Active
  • inmuDANCE Ref 5744000890067

    Class I EUDAMED Active
  • inmuRHYTHM Ref 5744000890197

    Class I EUDAMED Active

What inmutouch.com ApS makes

inmutouch.com ApS manufactures Class I medical devices for non-invasive neuromuscular stimulation, including the inmuJOY for targeted muscle activation, the inmuRELAX for relaxation therapy, the inmuDANCE for rhythmic muscle engagement, and the inmuRHYTHM for rhythm-based stimulation.

These devices are listed under the EU Medical Device Regulation (MDR) in the eudamed database as Class I products. The company is based in Denmark.

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 inmutouch.com ApS manufacture?

inmutouch.com ApS specializes in Class I medical devices focused on non-invasive neuromuscular stimulation. Their portfolio includes devices like the inmuJOY for targeted muscle activation, inmuRELAX for relaxation therapy, inmuDANCE for rhythmic muscle engagement, and inmuRHYTHM for rhythm-based stimulation. These devices are designed to interact with the body’s neuromuscular system without invasive procedures.

Where is inmutouch.com ApS based, and how does that affect its regulatory standing?

inmutouch.com ApS is based in Denmark, which is part of the European Union. Since their devices fall under the EU Medical Device Regulation (MDR), they are required to comply with EU-wide regulatory requirements. Their devices are listed in the eudamed database, which is the official EU registry for medical devices, ensuring transparency and traceability under EU law.

Are inmutouch.com ApS devices listed in any regulatory registries, and why does this matter?

Yes, inmutouch.com ApS devices are listed in the eudamed database, the official EU registry for medical devices. This matters because eudamed provides a centralized, publicly accessible record of devices authorized under the EU MDR, helping healthcare professionals, regulators, and patients verify compliance and traceability. Listing in eudamed ensures transparency and adherence to EU regulatory standards.

How are inmutouch.com ApS devices classified under EU regulations, and what does that classification mean?

inmutouch.com ApS devices are classified as Class I under the EU MDR. This classification is the lowest risk tier for medical devices and typically applies to items like bandages, gloves, or non-invasive neuromuscular stimulators like those produced by the company. Class I devices still require compliance with EU regulations, including proper labeling, risk management, and registration in eudamed, but they do not require pre-market approval or rigorous clinical trials like higher-risk classes.

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

Information

Country
Denmark
Address
20, Klakring Stationsvej, Juelsminde, Denmark
Website
inmutouch.com
Phone
+45 51955040
PRRC contact
Anders Hansen
EUDAMED SRN
DK-MF-000020064