What it's about
As medical devices in risk class IIa, ARTROMOT devices are subject to mandatory STK inspections.
Regular maintenance significantly extends the service life of ARTROMOT devices.
WINTER Medizintechnik is the official authorized distributor for ARTROMOT in Switzerland.
Only original spare parts and authorized service partners ensure safety and function.
Investing in maintenance not only protects patients, but also saves costs and resources.
Why proper device maintenance for CPM devices is essential
A CPM device (Continuous passive motion) performs precise work every day in postoperative rehabilitation. It moves operated joints gently and in a controlled manner, hour after hour, day after day. The fact that such a device functions reliably, safely, and accurately is not something that can be taken for granted. It is the result of consistent and professionally performed maintenance.
At WINTER Medizintechnik AG, we support ARTROMOT devices, some of which have been in use for 10 to 15 years and still function perfectly today. This is no coincidence. It is the direct result of regular, professionally performed service work.
ARTROMOT®: Quality made in Germany
ARTROMOT® CPM devices are manufactured in Germany and stand for the highest processing quality. The devices are robustly designed, precisely calibrated, and built for a long life cycle.
High-quality materials, precise mechanics, and reliable electronics form the foundation. Proper care is the decisive factor that preserves this quality over the long term. Well-maintained systems can significantly extend their service life and proactive maintenance reduces unplanned failures.
Legal basis: STK obligation for risk class IIa
ARTROMOT CPM devices are classified as medical devices in risk class IIa. Swiss law does not prescribe a fixed maintenance frequency. However, it does require that devices be maintained in accordance with the manufacturer's specifications, that inspections be carried out on a risk-based basis and at regular intervals, and that all measures be fully documented. The safety check (STK) is the central instrument here: It ensures that safety-relevant parameters are regularly checked, documented, and corrected if necessary. Incorrect angle values or electrical deviations can endanger the health of patients.
Operators of ARTROMOT devices, whether hospitals, rehabilitation clinics, or physiotherapy facilities, are legally obligated to comply with these regulations.
What professional maintenance includes
Properly performed maintenance of an ARTROMOT device is more than a superficial visual inspection. It typically includes the following points:
Mechanical inspection: Checking all moving parts for wear, play, and function.
Electrical safety test: Inspection of cables, plugs, insulation, and protective conductor connections.
Calibration: Checking and adjusting the angle settings and torque limiters.
Cleaning and lubrication: Removal of deposits and lubrication of relevant mechanical components.
Software check: Inspection of the control electronics.
Documentation: Recording all inspection steps and findings for the legally required device documentation.
If these steps are carried out at the prescribed intervals, the device not only remains safe, it remains reliable in use for many years.
WINTER Medizintechnik AG: Official authorized distributor for ARTROMOT® in Switzerland
As the official authorized distributor for ARTROMOT® in Switzerland, WINTER Medizintechnik AG is the central point of contact for all questions relating to spare parts, technical information, and service support.
Our technical support services include:
Delivery of original spare parts for all common ARTROMOT® device models in Switzerland.
Technical consulting on maintenance, repair, and correct operation of the devices.
Provision of service manuals and technical documentation for authorized service partners and technicians.
Our spare parts and technical information are regularly used by service partners and technicians in Swiss hospitals and clinics. Technicians from large service organizations that work in hospitals, including HOSPITEC AG and HERMED Medizintechnik Schweiz AG, are also in regular contact with us. Do you need spare parts or technical documents? Submit an inquiry directly now.
Through direct access to original spare parts and manufacturer documentation, we ensure that service work on ARTROMOT® devices can be carried out professionally, efficiently, and in accordance with the manufacturer's specifications.
Longevity as an economic and ecological advantage
An ARTROMOT® device that functions reliably for 10 or 15 years is an investment that pays off. The acquisition costs are spread over a long useful life. Regular maintenance costs are low compared to the costs of an unplanned failure or premature device replacement. Those who maintain consistently protect their budget.
In addition, a long-lasting device conserves resources. Fewer new purchases mean less production effort and less electronic waste. Sustainability therefore also begins with device care.
Recommendations for operators of ARTROMOT devices
Whether you operate ARTROMOT devices in a clinic, a rehabilitation facility, or in the home care sector: The following points will help you comply with legal requirements and maximize the service life of your devices.
Observe maintenance intervals: Have your devices maintained at the intervals prescribed by the manufacturer and the Swiss legislature.
Use only original spare parts: Non-original spare parts can impair safety and function and may void warranty claims.
Commission authorized service partners: Technicians should have access to up-to-date service manuals and manufacturer information.
Maintain device documentation: All maintenance and repair work must be fully documented.
Contact us directly if you have questions: As the official authorized distributor, WINTER Medizintechnik AG supports service partners and technicians quickly and competently.
Conclusion: Maintenance protects patients, conserves resources, and saves costs
ARTROMOT CPM devices are precision devices made in Germany with a long service life, provided they are maintained correctly. In Switzerland, regular safety check for risk class IIa devices is required by law. Anyone who takes this obligation seriously not only protects patients, but also significantly extends the useful life of their devices.
WINTER Medizintechnik AG is available as the official authorized distributor for ARTROMOT in Switzerland with original spare parts, technical documentation, and competent consulting. For hospitals, service technicians, and rehabilitation facilities, this provides direct and reliable access to everything needed for proper device care.
Do you have questions about spare parts, technical documentation, or maintenance of your ARTROMOT devices? Contact WINTER Medizintechnik AG directly. We provide fast, competent, and straightforward assistance. Submit an inquiry directly now.
