Poland
Medical device market intelligence for Poland. Regulatory changes, competitor moves, and procurement trends.
Recent signals
A completed multicenter trial in Poland, Romania, and Slovakia evaluated the safety and performance of SiPore21®.
The completed J-PET trial demonstrates a new PET scanner using plastic scintillators for improved imaging diagnostics.
WHO's first Global Forum unites over 800 Collaborating Centres to enhance scientific collaboration for public health.
A clinical trial is recruiting to compare 3D-printed stent-grafts with custom-made devices for aortic aneurysms.
Philips recalls ALLURA Xper FD20 OR Table due to intermittent X-ray imaging issues with the foot switch.
Mentor Texas, LP. recalls Class II Artoura Breast Tissue Expanders due to potential blunt needle tips.
Medtronic MiniMed's Paradigm Insulin Pumps are recalled due to risks of insulin over- and under-delivery affecting patient safety.
Mentor Texas, LP. recalls Class II CPX 4 US Breast Tissue Expanders due to potential blunt needle tips.
Philips recalled Azurion 5 M12 due to intermittent X-ray imaging issues with the wired foot switch.
Medtronic's MiniMed 620G insulin pump recalled due to risks of insulin over- and under-delivery affecting patient safety.
Mentor Texas recalls Class II CPX 4 US Breast Tissue Expanders due to potential blunt needle tips.
Medtronic's Paradigm REAL-Time Veo Insulin Pump recalled due to insulin delivery errors causing severe health risks.
Medtronic MiniMed's Paradigm REAL-Time Insulin Pumps are recalled due to insulin delivery issues causing severe health risks.
Medtronic's MiniMed 720G insulin pumps recalled due to risks of insulin over- and under-delivery affecting patient safety.
Mentor Texas, LP. recalls CPX 4 US Breast Tissue Expanders due to potential blunt needle tips affecting usage.
Philips recalled ALLURA Xper FD10F due to intermittent X-ray imaging issues with the wired foot switch.
Philips recalls Allura Xper FD20/10 due to intermittent X-ray imaging issues with the wired foot switch.
Philips recalls Azurion 7 B20 due to intermittent X-ray imaging issues with the wired foot switch.
Philips recalls Azurion 3 M12 due to intermittent X-ray imaging issues with the wired foot switch.
Philips recalls ALLURA Xper FD20 Biplane OR Table due to intermittent X-ray imaging issues with the foot switch.