Pure Global AI
Ireland flag

Ireland medical device registration timeline

Source-linked clocks

Health Products Regulatory Authority (HPRA) review clocks and end-to-end planning ranges, using the 4-class (I, IIa, IIb, III) — EU MDR classification system.

1 pathways1 of 1 clocks verifiedvalidity 5 years (CE certificate)MDSAP not acceptedreviewed 2026-08-29eur-lex.europa.eu
Class / pathwayReview clockPlanning totalWith prior approvalProvenance
Class I(Self-declaration (no notified body))
MDR Art. 52(7): non-sterile, non-measuring, non-reusable-surgical Class I devices are self-declared, so no authority or notified body reviews the file and there is no review clock
0 days6-9 monthsVerified
Review clocks exclude applicant hold time · planning totals are estimates

Ireland Medical Device Registration Process

Step-by-step HPRA registration process. Total estimated timeline: 6-9 months.

Step 1: Pre-Submission Preparation

1-3 months

Gather technical documentation, quality management system (QMS) records, and clinical data required by HPRA. Appoint a EU Authorized Representative.

Step 2: Application Submission

1-2 weeks

Submit complete registration dossier to HPRA including device description, risk analysis, and testing reports.

Step 3: Administrative Review

2-4 weeks

HPRA reviews application for completeness. May request additional documents or clarifications.

Step 4: Technical Evaluation

0 days

In-depth technical assessment of device safety and performance. HPRA may issue questions.

Step 5: Registration Approval

1-2 weeks

Upon successful review, HPRA issues Ireland market authorization certificate.

Summary: The Ireland medical device registration process through Health Products Regulatory Authority (HPRA) consists of 5 main steps: Pre-Submission Preparation → Application Submission → Administrative Review → Technical Evaluation → Registration Approval.
Prior approval recognition
FDA 510(k)/PMANo substitute for EU MDR conformity assessment; useful as predicate documentation in the technical file
Key requirements
  • EU Authorized Representative (for non-EU manufacturers)
  • EUDAMED and national economic-operator registration processed within 10 working days
  • MDR Art. 62 clinical investigations: validation 10-15 calendar days, outcome within 45 calendar days of validation (+20 with experts), sponsor response time excluded (AUT-G0095-7)
  • IVDR performance studies: validation on receipt, outcome within 45 calendar days (+20); Art. 58(1) studies without major clinical-risk procedures may commence after validation, others after authorisation (AUT-G0176-2)
Primary regulator sources

Reviewed 2026-08-29. End-to-end totals remain planning estimates.

Keep researching this market
View the Ireland resource hub →
Compare timeline across all countries →
Source-linked review clocks verified against HPRA publications · full review 2026-08-29 · row IDs are stable — cite as registration-timeline:ireland:class-i