We are a manufacturer of telemedicine systems
with a specific focus on telecardiology
The teleEKG® system, developed by our company, has enjoyed the recognition and satisfaction of users for 28 years.
Our offer includes
solutions for cardiac telerehabilitation, long-term cardiac telemonitoring, chronic disease telemonitoring and telecare.
The teleEKG® system developed by Pro-PLUS is in operation in many health care units in Poland and abroad.
The teleEKG® system is used throughout Poland
entific and medical institutes:
- Institute of Cardiology (Anin) in Warsaw
- Institute of Psychiatry and Neurology in Warsaw
- Institute of Biomedicine and Biocybernetics in Warsaw
- Military Medical Institute in Warsaw
Provincial and specialized hospitals:
- M. Kopernik Regional Specialist Hospital in Lodz, Poland
- Krakow's John Paul II Specialist Hospital
- Upper Silesian Medical Center Hospital in Ochojec
Academic centers and universities:
- Warsaw Medical University
- Academic Hospital in Umea, Sweden
- Medical University of Lodz
- Pomeranian Medical Academy in Szczecin
Private companies providing cardiology services:
- Cardiac Monitoring Center KARDIOFON in Warsaw
- CORDIUM in Warsaw
- MedGo Sp. z o.o.
- eMedicina Sp. z o.o.
- Telemedicine Poland S. A.
- American Heart of Poland S.A.
Our teleEKG® system also works internationally
Among others, in medical facilities in:
- Sweden
- Romania
- Czech Republic
- Ukraine
Scientific cooperation
Pro-PLUS implements and cooperates in the implementation of numerous scientific and research projects funded, among others, by NCBiR, such as Strategmed I and Strategmed II.
CE certification for medical devices
Pro-PLUS solutions are the highest quality medical devices with CE certification for both cardiac telemonitoring and rehabilitation products: EHO12, EHO-MINI Event Holter, EHO-MINI Event Rehabilitation, and CardioSCP and CardioSCP Web software.The certificate confirms compliance with the requirements of the Medical Devices Directive 93/42/EEC. Supervision of Pro-PLUS’ assurance of compliance of the products with the requirements of legislation and standards for medical devices is carried out by the notified body TUV NORD Polska Sp. z o.o. – unit number 2274.
Pro-PLUS operates in accordance with ISO 13485 and ISO 9001 quality standards.