Medical Device Alert Site Mhra.Gov.Uk

Alerts, recalls and safety information: drugs and medical …

https://www.gov.uk/drug-device-alerts

The MHRA is aware of cases of increased intraocular pressure in patients recently implanted with EyeCee One preloaded and EyeCee One Crystal preloaded intraocular …

Medical device safety information produced by the …

https://www.gov.uk/drug-device-alerts/medical-device-safety-information-produced-by-the-mhra

The MHRA is accredited to publish National Patient Safety Alerts (NatPSA) for medical devices and medicines. These alerts are sent to the NHS in England. The …

Report a problem with a medicine or medical device

https://www.gov.uk/report-problem-medicine-medical-device

Report a suspected problem (‘adverse incident’) with a medicine or medical device using the Yellow Card Scheme as soon as possible, for example if: a medicine causes side …

Regulating medical devices in the UK - GOV.UK

https://www.gov.uk/guidance/regulating-medical-devices-in-the-uk

Medical Devices Safety Bulletin (MDSB/2020/01) - GOV.UK

https://www.gov.uk/drug-device-alerts/medical-devices-safety-bulletin-mdsb-2020-01

a medical device including diagnostic tests, software and apps defective medicine (not of an acceptable quality) falsified or fake medicine or medical device side …

Yellow Card | Making medicines and medical devices safer

https://yellowcard.mhra.gov.uk/

Welcome to the Yellow Card reporting site. Report suspected side effects to medicines, vaccines, e-cigarettes, medical device incidents, defective or falsified (fake) products to …

Medical Device Alert - GOV.UK

https://assets.publishing.service.gov.uk/media/5eff0770d3bf7f76945f0c00/MDA-2020-019_Final_new.pdf

Devices Clinical Team, MHRA Tel: 020 3080 7274 Email: [email protected] To report an adverse incident involving a medical device in England use the Yellow Card reporting …

Alerts Relating to Medical Devices | Department of Health

https://www.health-ni.gov.uk/articles/medical-device-alerts-mdas

The Medicines and Healthcare products Regulatory Agency (MHRA) is now an accredited issuer of National Patient Safety Alerts, a format devised by NHS England. National …

Medical Device Alert - GOV.UK

https://assets.publishing.service.gov.uk/media/5954ca1ded915d0baa00009b/MDA-2017-018_Final.pdf

Alerts in Northern Ireland are distributed via the NI SABS system. Enquiries and adverse incident reports in Northern Ireland should be addressed to: Northern Ireland Adverse …

New UK MHRA Medical Devices Regulations Published - NAMSA

https://namsa.com/uk-mhra-medical-device-regulations-published/

New UK MHRA Medical Devices Regulations Published | NAMSA On 26 June 2022, the United Kingdom’s Medical Devices and Healthcare Regulatory Authority …