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MHRA Medical Device Safety Information – MDSI2307
MDSI2307 - EyeCee One and EyeCee One Crystal preloaded intraocular lenses: update of previous quarantine advice after identification of likely cause
Unique device identifiers: safety, monitoring & recalls
Find out more about unique device identifiers.
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
Device Safety Information – DSI/2025/001
DSI/2025/001- Suzhou Surgicare disposable Hysteroscopy Sheath – recall due to withdrawn CE certificate
MHRA Medical Device Safety Information – MDSI2406U2
MDSI2406U2 - Philips Respironics BiPAP A series ventilators: alarm malfunction and risk of therapy interruptions in ventilators not intended for life-
Information Message - IM/2021/002
IM/2021/002 - MHRA Device Expert Advisory Committee (DEAC): November minutes
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)