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MHRA Device Safety Information – MDSI (SC) 2104
MDSI (SC) 2104 - Total parenteral (TPN) and enteral nutrition bags manufactured by Diffuplast: Sterilisation issue
MHRA Device Safety Information – MDSI (SC) 2106
MDSI (SC) 2106 - Investigation update: CE mark suspended for all MAGEC systems manufactured by NuVasive Specialized Orthopedics, Inc.
MHRA Device Safety Information - MDSI (SC) 2101
MDSI (SC) 2101 - Paclitaxel drug-coated balloons (DCBs) or drug-eluting stents (DESs)
MHRA Device Safety Information – MDSI (SC) 2102
MDSI (SC) 2102 - Medoject sterile hypodermic and blunt fill needles manufactured by Chirana T. Injecta – discontinue use
Safety Action Notice - SAN(SC)21/07
SAN(SC)21/07 - Nitri-Hand non-sterile nitrile examination glove, product codes: FTG813, FTG814, FTG815, FTG816, FTE9936, FTE9940, FTE9941
Safety Action Notice - SAN(SC)21/06
SAN(SC)21/06 - Duraweld face visors, Ref EPVS0143, manufactured up to 13 July 2020: latex warning
Safety Action Notice - SAN(SC)21/03
SAN(SC)21/03 - Oxygen Supply (COVID-19)
Safety Action Notice - SAN(SC)21/04
SAN(SC)21/04 - RWC TMV3 Easifit 15mm T-type thermostatic mixing valves: elevated mixed water outlet temperatures under certain conditions
Safety Action Notice - SAN(SC)21/05
SAN(SC)21/05 - Fang Tian FT-045A FFP3 respirators supplied by Polyco Healthline, product code BWM541
Safety Action Notice - SAN(SC)20/07
SAN(SC)20/07 - Foreign body aspiration during intubation, advanced airway management or ventilation