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National Patient Safety Alert - NatPSA/2021/005/MHRA
NatPSA/2021/005/MHRA - Philips ventilator, CPAP and BiPAP devices: Potential for patient harm due to inhalation of particles.
Information Message - IM/2020/022
IM/2020/022 - Regulation of medical devices and in-vitro diagnostic medical devices
Safety Action Notice - SAN2306
SAN2306 - Medical devices intended for use in a sterile state: review of systems and procedures
MHRA Medical Device Safety Information – MDSI2403
MDSI2403 - Counterfeits and unbranded copies of LifeVac anti-choking devices may fail to work correctly or worsen choking incidents if used.
MHRA Medical Device Safety Information – MDSI2310
MDSI2310 - SteriFeed Colostrum Collection device and risk of choking due to infant airway occlusion.
MHRA Medical Device Safety Information – MDSI2406
Philips Respironics BiPAP A series ventilators: alarm malfunction and risk of therapy interruptions in ventilators not intended for life-support
MHRA Medical Device Safety Information – MDSI2407
MDSI2407 - Zimmer CPT Hip System Femoral Stem 12/14 Neck Taper: increased risk of postoperative periprosthetic femoral fracture
MHRA Medical Device Safety Information – MDSI2311U
MDSI2311U - Specific brands of carbomer eye gel: recall of AACARB eye gel, AACOMER eye gel and PUROPTICS eye gel: potential risk of infection - UPDATE
MHRA Medical Device Safety Information – MDSI2405
MDSI2405 - Symbios ORIGIN® Posterior Stabilised Patient-Matched Total Knee Replacement Device: Risk of Early Revision
MHRA Medical Device Safety Information – MDSI2404
MDSI2404 - Legency Remedies 0.9% Sodium Chloride Solutions for Irrigation, Inhalation, and Eyewash: risk of microbiological contamination