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  • Register medical devices to place on the market - GOV. UK
    UK manufacturers who do not already have a Device Online Registration System (DORS) account must create one and register their custom-made devices You only need one DORS account to register
  • Regulating medical devices in the UK - GOV. UK
    All medical devices, including IVDs, custom-made devices and systems or procedure packs must be registered with the MHRA before being placed on the Great Britain market
  • 2026 UK MHRA Registration: Step-by-Step Guide - Casus Consulting
    Who is allowed to submit UK registrations? The MHRA medical device registration can only be completed by companies located in the UK: either UK manufacturers or a foreign manufacturer’s UK Responsible Person (UKRP) Further, it must be completed in the MHRA’s online database, called ‘DORS’
  • Unsure how to register with the MHRA DORS? - Deviceology
    You must ensure all information registered with the MHRA is accurate and up to date To do this you first need to register your organisation with a manufacturer’s account with the MHRA’s Device Online Registration Service (DORS)
  • PARD
    The MHRA public access registration database (PARD) website allows you to find: Registration of medical devices with the MHRA (the UK Competent Authority) does not represent any form of
  • Medical Device MHRA Registration UK Guide 2025 | RRC
    DORS is the MHRA’s online portal for registering all medical devices for the Great Britain market UK-based manufacturers and UKRPs for non-UK manufacturers must use DORS before placing devices on the market
  • UK MHRA 2026 Overhaul: CE Mark Recognition, DORS Fees and Clinical . . .
    Effective April 1, 2026, the MHRA replaced its one-off device registration fee with an annual fee model under the Devices Online Registration System (DORS) This is a fundamental change in how manufacturers are charged for maintaining their medical device registrations in the UK
  • MHRA registration updates: What they mean for your… | G L Scientific
    The guidance, released on 17 February 2025, explains how to navigate these changes using the MHRA’s Device Online Registration System (DORS) As timelines under the EU Medical Devices Regulation (EU MDR 2017 745) shift, understanding the implications for UK registrations is critical
  • Guidance: Device registration fee - GOV. UK
    We have strengthened our safety and surveillance system for medical devices following the post-market surveillance legislation (SI 2024 No 1368) that came into force on 16 June 2025
  • A 2025 Guide For UK Medical Device Registration Process- Sushvin . . .
    This blog outlines the step-by-step process for registering medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) —including key timelines, roles, and compliance expectations





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