Poland
Medizinprodukt-Marktintelligenz für Poland. Regulatorische Änderungen, Wettbewerber und Beschaffungstrends.
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The SANIFORM-II positioning cushion by MULTITEX is classified as a Class I medical device with UDI-DI 05902675096034.
Hygomed Disposable Dental Trays by Metzer Medizin are registered as Class I medical devices.
The VIDA BELA 25G dermatological cannulas are classified as Class IIa medical devices by Medical Brokers Adam Cieślak.
The clinical investigation of 'Alexa Volume' showed significant aesthetic improvements and a favorable safety profile.
The SuMRI tracheostomy tube with cuff is classified as Class IIB and registered by SUMI.
The PURE device by INEOCARE is classified as Class I and registered in EUDAMED with UDI-DI 05903899903559.
The device PB521IIL-4C-120190-P by Elbur is classified as Class I and has a UDI-DI of 05904261347414.
The device PB521IIL-4C-90197-I-VMH-Z4 by Elbur is registered as Class I in EUDAMED.
Elbur's PB521IIL-4C-120200-P is a Class I medical device registered in EUDAMED.
The device PB521IIL-4C-90190-I-VMH by Elbur is classified as Class I and registered in EUDAMED.
The ZenFlex orthopedic pillow by GOODWILL BRANDS is classified as a Class I medical device.
The ZenFlex orthopedic cushion by GOODWILL BRANDS is classified as a Class I medical device.
SteriPack Medical Poland has registered a medical device with product code HEM with the FDA.
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.