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Safety Action Notice - SAN2306
SAN2306 - Medical devices intended for use in a sterile state: review of systems and procedures
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
Safety Action Notice - SAN(SC)19/03
SAN(SC)19/03 - Risk of death and severe harm from ingesting superabsorbent polymer gel granules.
Estates and Facilities Notices - EFA/2019/004
EFA/2019/004 - Zebra printer Power Supply Units (PSUs): fire risk – product recall expanded
Estates and Facilities Notices - EFA/2019/003
EFA/2019/003 - ‘Anti-ligature’ type curtain rail systems: Risks from incorrect installation or modification
MHRA Medical Device Safety Information – MDSI2406U
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 – MDSI2403
MDSI2403 - Counterfeits and unbranded copies of LifeVac anti-choking devices may fail to work correctly or worsen choking incidents if used.
Multi-drug resistant organism admission screening
Find guidance about MDRO
Guidance on Safe Management of Medical Devices and Equipment in Scotland’s Health and Social Care Services (SHTN 00-04)
This guidance is intended to support safe and effective medical devices and equipment risk management practice in health and social care services.
MHRA Medical Device Safety Information – MDSI2405
MDSI2405 - Symbios ORIGIN® Posterior Stabilised Patient-Matched Total Knee Replacement Device: Risk of Early Revision