I will do UK mhra registration for medical devices and ivds

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

Selling medical devices in the UK without MHRA registration means customs holds, pulled listings, and lost revenue. Get it right once, and you're cleared to sell.

I'm a regulatory consultant handling UK, EU, and US medical device submissions for manufacturers, importers, and distributors across Class I, IIa, IIb, and IVDs.

What you get:

• Device classification under UK MDR 2002
• GMDN code identification
• Technical documentation review and gap analysis
• UK Responsible Person guidance for non-UK manufacturers
• Full MHRA DORS submission
• Post-submission tracking until confirmation

Who this is for: 

Manufacturers, importers, and distributors placing medical devices or IVDs on the UK market especially non-UK companies needing a clear, compliant path in.

Before ordering, please message me with:

1. Device name and intended use
2. Risk class (if known)
3. Your role: manufacturer / importer / distributor
4. Country of origin

I'll confirm scope, timeline, and the right package for your case.

• Note: Required documentation must be supplied by the company. MHRA approval timelines are set by the agency.