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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 – MDSI2310
MDSI2310 - SteriFeed Colostrum Collection device and risk of choking due to infant airway occlusion.
Decontamination - Guidance on loan devices (GUID 5002)
National Decontamination Guidance on Loan Medical Devices (Reusable): Roles & Responsibilities GUID 5002
Further reading
IRIC Further reading