Ireland
Intelligence de marché des dispositifs médicaux pour Ireland. Changements réglementaires, concurrents et tendances d'achats.
Signaux récents
Abbott Laboratories has registered three medical devices under product code QBJ with the FDA.
Tcoag Ireland Limited has FDA registration 3008386529 for a product under code DAP.
The Baska mask, a new supraglottic airway device, has been assessed against the LMA in a completed study.
A completed UK & Ireland audit assessed MS patient adherence to Rebif® injections using the RebiSmart™ device.
A completed study assessed compliance and satisfaction with the Lenire bimodal stimulation device for tinnitus treatment.
Over half of women with gestational diabetes face harmful stigma affecting their well-being, according to new research.
The PhenMap tool predicts bowel cancer patients' responses to a new NHS drug, potentially sparing ineffective treatments.
Manna, an Irish drone delivery startup, secured $50M to expand operations in the U.S. and Europe, totaling $110M funding.
The ATTUNE KNEE SYSTEM by DePuy Ireland UC is classified as a Class I medical device.
The ATTUNE KNEE SYSTEM by DePuy Ireland UC is classified as Class I and registered with UDI-DI 10603295505051.
The ATTUNE device by DePuy Ireland UC is classified as Class IIB and registered with UDI-DI 10603295520801.
Omni raised $120 million to address enterprise data translation issues, valued at $1.51 billion post-funding.
The Windsor Framework outlines pharmacovigilance protocols for medical devices post-agreement.
Iterum Therapeutics is winding down due to limited cash and poor sales of its antibiotic Orlynvah.
WHO's first Global Forum unites over 800 Collaborating Centres to enhance scientific collaboration for public health.
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.