I will do UK mhra registration for medical devices and ivds

P
profga
P
profga
gary

About this gig

MHRA Registration Done Right for Medical Devices, IVDs & Surgical Tools

Selling medical devices in the UK without the right MHRA registration can lead to customs delays, marketplace issues, and lost revenue. Get your registration process organized correctly from the start.

Im a regulatory consultant providing support for UK, EU, and US medical device submissions for manufacturers, importers, and distributors, covering Class I, IIa, IIb, and IVDs.

What You Get

  • Medical device classification under UK MDR 2002
  • GMDN code identification
  • Technical documentation review & gap analysis
  • UK Responsible Person guidance for non-UK manufacturers
  • MHRA DORS submission support
  • Post-submission tracking through confirmation

Who This Service Is For

Manufacturers, importers, and distributors placing medical devices or IVDs on the UK market especially non-UK companies looking for a clear path through the registration process.

Before Ordering

Please message me with:

  1. Device name & intended use
  2. Risk class, if known
  3. Your role: Manufacturer / Importer / Distributor
  4. Country of origin

Ill review your requirements and confirm the scope, timeline, and most suitable package for your case.

Get to know gary

gary

Profesional services

  • FromUnited States
  • Member sinceAug 2026
  • Languages

    English
Perhaps you found me for a reason. Some projects need more than someone who can simply get the job done. They need vision, precision, discretion, and an instinct for what makes the difference. I take ideas, requirements, and unfinished concepts and turn them into work that feels intentional — polished, distinctive, and difficult to overlook. No unnecessary promises. No noise. No complicated process. Just focused execution, quiet confidence, and a result that speaks for itself. If you know what you’re looking for, you already know why you’re here.