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MHRA Medical Device Safety Information – MDSI2311
MDSI2311 - Specific brands of carbomer eye gel: recall of AACARB eye gel, AACOMER eye gel and PUROPTICS eye gel – potential risk of infection
MHRA Medical Device Safety Information – MDSI2309
MDSI2309 - BioIntegral Surgical Inc. No-React® cardiovascular bioprosthesis implantables: discontinuation of CE marking and manufacture
MHRA Medical Device Safety Information – MDSI2308
MDSI2308 - Ethypharm Aurum pre-filled syringes are incompatible with some needle-free connectors: risk of delay of potentially lifesaving medication
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DSI/2025/001- Suzhou Surgicare disposable Hysteroscopy Sheath – recall due to withdrawn CE certificate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-
Device Safety Information – DSI/2025/002
DSI/2025/002 - Aurum pre-filled syringes phased introduction of new 10ml CONNECT syringe barrel
Information Message - IM/2021/002
IM/2021/002 - MHRA Device Expert Advisory Committee (DEAC): November minutes