Ministry of Public Health market accessUruguay medical device registration resources
Research Ministry of Public Health registration records, classification, regulations, timelines, fees, and market updates — the stable entrance to every Uruguay medical device resource.
Everything we track for Uruguay
Browse by resource instead →Additional certification and licence checker
Check whether product features may trigger separate radio, electrical, metrology, radiation, import, or other Uruguay requirements.
Medical device regulation news
Follow recent Ministry of Public Health — Medical Technology Evaluation Department policy, guidance, safety, and compliance updates.
Registration timeline
Compare official and realistic MSP approval times by device class and pathway.
Government registration fees
Check current Ministry of Public Health fee requirements for device market entry.
Government fees
Full fee schedule (1 lines) →Ministry of Public Health registration fees in UYU · reviewed 2026-08-25
| Fee line | Amount | Provenance |
|---|---|---|
| PIRM registration and MSP arancelado fees (indexed UR units) | PIRM: 5 UR fixed + 25 UR families + professional stamps | Planning estimate |
Registration timeline
Full registration timeline →Ministry of Public Health (MSP) review clocks and planning ranges · Device registration under Decree 3/008 classification
| Class / pathway | Review clock | Planning total | Provenance |
|---|---|---|---|
| Medical-device registration(MSP registration) | 180 days | 7-10 months | Verified |
- 1Pre-Submission Preparation(1-3 months)
- 2Application Submission(1-2 weeks)
- 3Administrative Review(2-4 weeks)
- 4Technical Evaluation(180 days)
- 5Registration Approval(1-2 weeks)
Latest regulation news
All Uruguay regulation news →Newest Ministry of Public Health-related headlines from the daily-refreshed feed — every row links to the publishing source.
UruguayAug 26OSOperon StrategistSFDA Medical Device Establishment License (MDEL): Complete Compliance GuideUruguayAug 25MGMedEnvoy GlobalHow Does Mexico Classify Single-Use Versus Reusable Medical Devices?UruguayAug 25FLFDA Law BlogFDA Addresses Device Constituents in New Draft Guidance on Container Closure SystemsUruguayAug 25PBPacific BridgeCan Foreign Clinical Data be Used to Get Your Medical Device Approved in Japan?UruguayTurn Uruguay research into practical work
The target market is carried into each tool. Add the product, evidence, or regulatory change you want to assess.
Build a reusable product master
Structure company, product, model, approval, certificate, and evidence facts before starting Uruguay work.
Uruguay market-launch workpaper
Connect the Ministry of Public Health route, evidence, labels, local role, timing, and dependencies to a wider launch plan.
Uruguay dossier reuse and delta
Compare an existing authorization and evidence set against Ministry of Public Health administrative, testing, labeling, and dossier needs.
Uruguay change notification workpaper
Map a product or manufacturing change to Ministry of Public Health evidence, notification, timing, and implementation questions.
Uruguay regulatory change impact
Assess a current Ministry of Public Health update against one product and turn it into an owner-ready action workpaper.
Uruguay cybersecurity evidence review
Review connected-device architecture, risks, SBOM, testing, lifecycle controls, and market-specific questions for Uruguay (Ministry of Public Health).
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