Mhra Registered Medical Devices

Register medical devices to place on the market - GOV.UK

https://www.gov.uk/guidance/register-medical-devices-to-place-on-the-market

All medical devices, including IVDs, custom-made devices and systems or procedure packs must be registered with the MHRA before they can be placed on the Great Britain market. From 1 January 2022 ...

Regulating medical devices in the UK - GOV.UK

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

Factsheet: medical devices overview

https://www.gov.uk/government/publications/medicines-and-medical-devices-bill-overarching-documents/factsheet-medical-devices-overview

There are approximately 600,000 medical devices available on the UK market. The Medicines and Healthcare products Regulatory Agency (MHRA) is responsible for ensuring …

Public Access Database for Medical Device Registration

https://aic.mhra.gov.uk/era/pdr.nsf/name?openpage&start=1&count=200

Date Registered MHRA Reference Number Devices; 121 Dental Laboratory: …

Public Access Database for Medical Device Registration

https://aic.mhra.gov.uk/era/pdr.nsf/Search?openform

MHRA Reference Number: By Device Name: Contact details. Freedom of information. 020 3080 7272 (manned 10:00-16:00 hours working days) [email protected]

MHRA | MHRA - Medicines and Healthcare products …

https://cms.mhra.gov.uk/mhra

Welcome to MHRA-GMDP The MHRA-GMDP database contains the following information issued by the MHRA relating to manufacturing and wholesale authorisations and …

New UK MHRA Medical Devices Regulations Published - NAMSA

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

On 26 June 2022, the United Kingdom’s Medical Devices and Healthcare Regulatory Authority (MHRA) published the results and conclusions from the consultation …

Medical device safety information produced by the MHRA

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

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

Notify the MHRA about a clinical investigation for a …

https://www.gov.uk/guidance/notify-mhra-about-a-clinical-investigation-for-a-medical-device

Day 1 of the MHRA assessment is taken as being the date that we confirm that we have received a valid application. During the assessment experts will assess the …

MHRA Products | Search results

https://products.mhra.gov.uk/search

Products. **STATUS UPDATE** We apologise for any inconvenience as we are currently experiencing technical difficulties with adding, updating or deleting all SPCs and PILs. …