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Incident Reporting and Investigation Centre Conference
Find information on our annual IRIC conference for Scotland health and social care professionals.
When to report an incident to us
Information about when you should report an adverse incident.
Decontamination of medical devices in a Central Decontamination Unit (SHTM 01-01)
Scottish Health Technical Memorandum 01-01 Parts A, B, C, D, E and F, GUID 5017 and 5019: decontamination of medical devices processed through a CDU.
National Patient Safety Alert – NatPSA/2021/001/MHRA
NatPSA/2021/001/MHRA - Supply disruption of sterile infusion sets and connectors manufactured by Becton Dickinson (BD)
Water safety for emerging technologies (SHTM 04-02)
Scottish Health Technical Memorandum 04-02 Parts A, B and C: control of Legionella, hygiene, ‘safe’ hot water, cold water and drinking water.
Additional learning resources on TURAS
Additional learning resources include IRIC spotlight session recordings and medical device e-learning modules.
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) 2105
MDSI (SC) 2105 - Recall of BD Venflon Pro safety IV cannula
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.
Global Medical Device Nomenclature (GMDN) as a trending tool
Learn more about the GMDN – a medical device sorting machine.