Mexico
Intelligence de marché des dispositifs médicaux pour Mexico. Changements réglementaires, concurrents et tendances d'achats.
Signaux récents
A completed study evaluated the safety of PRO-149 vs. Healon® EndoCoat in cataract surgery.
Cordis US Corp. is registered with the FDA under product code DQY, owned by Cardinal Health Mexico.
DEROYAL CIENTIFICA DE LATINOAMERICA S.R.L. has FDA registration 9613793 for 2 products under code FMZ.
NOVEM MEDICAL S. DE R.L. DE C.V. has registered a medical device with product code CBH.
CALIBAJA MANUFACTURING, S.A. DE C.V. is registered with the FDA under product code EGD.
Jabil Inc. has registered with the FDA under product code GEX, listing one medical device.
A clinical trial is recruiting to assess the Aurora® device's efficacy in treating anxiety alongside medication.
Two CIA agents killed in Mexico were unauthorized for local operations, per Mexico's Ministry of Security.
ICU Medical, Inc. has registered a product with the FDA under code FPA.
GBA1 is identified as a major Parkinson's disease risk factor in West Africa, highlighting global research collaboration.
Affordability metrics for safe water and clean cooking fail to reflect true burdens in low-income countries.
FDA denies Regenxbio's gene therapy application for Hunter syndrome.
WHO's first Global Forum unites over 800 Collaborating Centres to enhance scientific collaboration for public health.
AI is revolutionizing TB screening with handheld X-ray devices in over 22 countries.
Bodycote will open a new heat treatment facility in Apodaca, Mexico to enhance local processing capacity.
Philips recalls ALLURA Xper FD20 OR Table due to intermittent X-ray imaging issues with the foot switch.
Burlington Medical recalls Class II protective sleeves due to potential lifespan degradation.
Medtronic MiniMed's Paradigm Insulin Pumps are recalled due to risks of insulin over- and under-delivery affecting patient safety.
Burlington Medical's Kilt Blockers recalled due to potential lifespan degradation, affecting worldwide distribution.
Burlington Medical recalls Class II Demi Half Aprons due to potential attenuation degradation affecting lifespan.