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MHRA Device Safety Information – MDSI2203
MDSI2203 - Paclitaxel drug-coated balloons or drug-eluting stents: updated position
MHRA Device Safety Information – MDSI2202
MDSI2202 - Surdial X Haemodialysis machine: potential for devices to remove excess fluid outside of machine specification
MHRA Device Safety Information – MDSI2201
MDSI2201 - Gemini Surgical UK: Stop using all lots and batches of vaginal speculums with smoke tube and gynaecological hysteroscopy sheaths
MHRA Device Safety Information – MDSI2110
MDSI2110 - Baihe Rheovalves disposable needle-free valves: stop using specific lots due to risk of breakage in patient
MHRA Device Safety Information – MDSI2109
MDSI2109 - Handpieces used in the phacoemulsification technique of cataract removal: need for careful cleaning (DSI/2021/009)
MHRA Device Safety Information – MDSI2108
MDSI2108 - Medical devices sterilised by Steril Milano - potential for incomplete sterilisation
MHRA Device Safety Information – MDSI2107
MDSI2107 - Recall of BD Venflon Pro safety and Venflon Pro IV cannula
The new EU Medical Devices Regulations
Find out about the legislation and regulations for medical devices and in-vitro diagnostic medical devices, and the Health Institution Exemption.
MHRA Device Safety Information (MDSI)
MHRA Device Safety Information (MDSI) MDSIs capture safety information from MHRA. The information is about safety concerns which do not meet MHRAs cri
Get in touch about the scheme
Get advice on the clinical negligence cover scheme for health boards. Contact our solicitors.