Astar ABR A. Jędrzejowski, R. Dziendziel S.J holds a certified quality management system according to EC Directive 93/42/EEC-MDD Annex II (except II.4), EN ISO 13485:2016 for design and development, production, distribution and servicing of active medical therapy devices for electrotherapy, laser therapy, light therapy, magnetic field therapy and ultrasound therapy.
Products in the scope of EC Directive 93/42/EEC-MDD Annex II (except II.4) are:
- Electrotherapy devices
- Laser therapy devices
- Light therapy devices
- Magnetic field therapy devices
- Ultrasound therapy devices
- Ultrasound therapy combined with electrotherapy devices
- Vacuum therapy devices
- Shock wave physical therapy devices
The quality management system of Astar ABR A. Jędrzejowski, R. Dziendziel S.J is subject to regular, annual monitoring by TÜV Rheinland Group.
Robert Dziendziel Spolka Jawna
ul. Swit 33