Saudi Arabia
Medizinprodukt-Marktintelligenz für Saudi Arabia. Regulatorische Änderungen, Wettbewerber und Beschaffungstrends.
Neueste Signale
The Delivery Pack by Enayah is a Class I medical device registered with UDI-DI 62811410273690.
CoMira Diagnostics has finalized a lease for a manufacturing facility in Sudair Industrial City, Saudi Arabia.
Korean medtech firms ROKIT and Seers partner with Middle East companies to expand AI-enabled health technologies.
AiZtech Labs launched iSelfie BioSignals in the U.S. to automate digital biomarker detection via smartphone selfies.
A completed study in the Middle East evaluated adherence to SAIZEN® using the Easypod™ device in pediatric patients.
Gulf rulers aim to enhance R&D to transform their economies, but the effectiveness of their plan remains uncertain.
Saudi Arabia may shift its security strategy towards China post-Iran conflict, but US ties limit broader cooperation.
The GCC is becoming structurally indispensable to the global economy despite geopolitical tensions.
WHO's first Global Forum unites over 800 Collaborating Centres to enhance scientific collaboration for public health.
Saudi Arabia commits $39 million to the Global Fund's Eighth Replenishment for global health initiatives.
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.
Siemens recalls Atellica CH A1c_E due to potential negative bias affecting diabetes diagnosis.
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.
BD Kiestra ReadA (Catalog No. 446948) recalled due to intermittent remote connectivity issues post-reboot.
Medtronic's Paradigm REAL-Time Veo Insulin Pump recalled due to insulin delivery errors causing severe health risks.