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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.
Detecting fraud in the public sector
How our experts work with partners from across Scotland's public sector to identify and defeat fraud.
Information Message - IM/2020/022
IM/2020/022 - Regulation of medical devices and in-vitro diagnostic medical devices
Safety Action Notice - SAN2306
SAN2306 - Medical devices intended for use in a sterile state: review of systems and procedures
MHRA Medical Device Safety Information – MDSI2403
MDSI2403 - Counterfeits and unbranded copies of LifeVac anti-choking devices may fail to work correctly or worsen choking incidents if used.
Decontamination - Guidance on loan devices (GUID 5002)
National Decontamination Guidance on Loan Medical Devices (Reusable): Roles & Responsibilities GUID 5002
Further reading
IRIC Further reading
MHRA Medical Device Safety Information – MDSI2310
MDSI2310 - SteriFeed Colostrum Collection device and risk of choking due to infant airway occlusion.
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