New Zealand
Intelligence de marché des dispositifs médicaux pour New Zealand. Changements réglementaires, concurrents et tendances d'achats.
Signaux récents
Wellumio raised $9.75M to commercialize its Axana portable brain imaging device for acute stroke detection.
A terminated study evaluated a modified PAP device's efficacy for obstructive sleep apnea against a market product.
Fisher & Paykel Healthcare NZ Ltd has registered product code CAW with the FDA.
Fisher & Paykel Healthcare NZ Ltd has registered a medical device with product code CAT.
The Airvo 3 device by Fisher and Paykel Healthcare is undergoing validation for respiratory rate monitoring accuracy.
The completed trial assessed CPAP device performance to meet user and clinical requirements.
Smoking remains a leading cause of death, with 480,000 U.S. deaths annually, despite declining smoker rates.
Medsafe in New Zealand is consulting on extending abbreviated procedures for new medicine applications.
Medsafe in New Zealand is consulting on rules for the consent by verification pathway for new medicines approval.
In 2024, 4.9 million children died before age five, with preventable causes dominating mortality rates.
The Access Consortium's 2026 plan aims to enhance collaboration and expedite access to innovative medicines for patients.
Philips recalls ALLURA Xper FD20 OR Table due to intermittent X-ray imaging issues with the foot switch.
Medtronic MiniMed's Paradigm Insulin Pumps are recalled due to risks of insulin over- and under-delivery affecting patient safety.
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.
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.
Philips recalled ALLURA Xper FD10F due to intermittent X-ray imaging issues with the wired foot switch.