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Development and manufacturing of devices for non-invasive home ventilation and respiratory therapy

JF

JFR Medical Instruments GmbH

Wasserwaage 8, 24226 Heikendorf, GermanyNew on Amplifa

2014Founded
11–50Employees
GmbHLegal form
Heikendorf, Schleswig-HolsteinHeadquarters

About JFR Medical Instruments

JFR Medical Instruments GmbH is a medical technology company based in Heikendorf, Schleswig-Holstein. Since 2014, the company has been developing and producing devices 'Made in Germany' for non-invasive home ventilation and respiratory therapy as well as solutions for sleep therapy. The product portfolio includes ventilators (Cube 30 ATV, eva), Android-based ventilation and sleep therapy devices (JETNOVA series), accessories and humidifiers. The products are aimed at patients in the homecare sector as well as medical professionals and are continuously further developed with a focus on ease of use, reliability and high standards. The company is certified according to EN ISO 13485 and fulfils the requirements of the Medical Device Regulation (EU 2017/745). It presents its products at international trade fairs such as the World Health Expo in Dubai and the ERS Congress.

Site
Heikendorf
Processes
Development and manufacture of non-invasive home ventilation and respiratory therapy devices, Sleep therapy solutions, Accessories for respiratory therapy
Certificates
EN ISO 13485, MDR (EU 2017/745) Compliance
Founded
2014
Employees
11–50
Industries
Medical Technology, Electromedical Devices, Respiratory/Homecare Care
  1. 01

    Development

  2. 02

    Production

  3. 03

    Quality Management

  4. 04

    Sales

Location

Heikendorf

DE

Headquarters with development and production

Industries

Medical TechnologyElectromedical DevicesRespiratory/Homecare Care

Additional services

Development and manufacture of non-invasive home ventilation and respiratory therapy devicesSleep therapy solutionsAccessories for respiratory therapy

Quality and Certification

The company is certified according to EN ISO 13485 and fulfils the requirements of the Medical Device Regulation (EU 2017/745) for medical devices.

EvidenceHeikendorf
EN ISO 13485
MDR (EU 2017/745) Compliance

History

  1. 2014

    Foundation and start of the development and production of devices for non-invasive home ventilation and respiratory therapy

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