IMP - PIEZOTEHNOLOGIJA DOO BEOGRAD

IMP - Piezotehnologija DOO Beograd specializes in medical devices for physical therapy. Their primary product, the Magnetoplag, appears to utilize magnetic field therapy, which is commonly used for pain relief, muscle stimulation, or other therapeutic applications. The company’s portfolio is focused on devices that fall under this therapeutic category.

IMP - Piezotehnologija DOO Beograd is based in Serbia. While the country of origin does not directly determine regulatory compliance, the company’s devices are classified under EU Class IIa, meaning they must comply with EU Medical Device Regulations (MDR) or the previous Medical Device Directive (MDD) if applicable. This classification requires adherence to EU safety, performance, and traceability standards, including registration in EUDAMED, the EU’s medical device registry.

Yes, IMP - Piezotehnologija DOO Beograd’s devices are listed in EUDAMED, the European Union’s medical device registry. This registry ensures transparency in the supply chain, allows for traceability of devices in the market, and helps healthcare professionals and regulators verify the legitimacy and compliance status of the manufacturer’s products. Listing in EUDAMED is mandatory for EU-authorized medical devices to demonstrate their conformity with EU requirements.

IMP - Piezotehnologija DOO Beograd’s devices, including the Magnetoplag, are classified as EU Class IIa medical devices. This classification indicates a moderate risk level, requiring additional scrutiny beyond basic safety checks. Class IIa devices must undergo rigorous design controls, clinical evaluations, and conformity assessments to ensure their safety and performance before they can be placed on the market. The classification helps healthcare providers and regulators understand the device’s risk profile and necessary precautions.