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MHRA Device Safety Information – MDSI2107
MDSI2107 - Recall of BD Venflon Pro safety and Venflon Pro IV cannula
The new EU Medical Devices Regulations
Find out about the legislation and regulations for medical devices and in-vitro diagnostic medical devices, and the Health Institution Exemption.
MHRA Device Safety Information (MDSI)
MHRA Device Safety Information (MDSI) MDSIs capture safety information from MHRA. The information is about safety concerns which do not meet MHRAs cri
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 – 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