Ministry of Health market accessOman medical device registration resources
Research Ministry of Health registration records, classification, regulations, timelines, fees, and market updates — the stable entrance to every Oman medical device resource.
Everything we track for Oman
Browse by resource instead →Additional certification and licence checker
Check whether product features may trigger separate radio, electrical, metrology, radiation, import, or other Oman requirements.
Medical device regulation news
Follow recent Ministry of Health — Drug Safety Center policy, guidance, safety, and compliance updates.
Registration timeline
Compare official and realistic MoH approval times by device class and pathway.
AI medical device classifier
Describe your device and get a preliminary MoH risk class with official rule references.
Government registration fees
Review current Ministry of Health application, review, and renewal fees.
Government fees
Full fee schedule (6 lines) →Ministry of Health registration fees in OMR · reviewed 2026-08-25
| Fee line | Amount | Provenance |
|---|---|---|
| Device registration - Class A/B | OMR 100 | Verified |
| Device registration - Class C/D | OMR 200 | Verified |
| Manufacturer registration - non-local manufacturer | OMR 500 | Verified |
| Manufacturer registration - local manufacturer | OMR 1,500 | Verified |
Registration timeline
Full registration timeline →Oman Ministry of Health (MoH) review clocks and planning ranges · 4-class (A, B, C, D) — GCC-aligned classification
| Class / pathway | Review clock | Planning total | Provenance |
|---|---|---|---|
| Medical-device registration service(MoH registration) | 60 working days | 3-5 months | Verified |
- 1Pre-Submission Preparation(1-3 months)
- 2Application Submission(1-2 weeks)
- 3Administrative Review(2-4 weeks)
- 4Technical Evaluation(60 working days)
- 5Registration Approval(1-2 weeks)
Latest regulation news
All Oman regulation news →Newest Ministry of Health-related headlines from the daily-refreshed feed — every row links to the publishing source.
OmanAug 26OSOperon StrategistSFDA Medical Device Establishment License (MDEL): Complete Compliance GuideOmanAug 25MGMedEnvoy GlobalHow Does Mexico Classify Single-Use Versus Reusable Medical Devices?OmanAug 25FLFDA Law BlogFDA Addresses Device Constituents in New Draft Guidance on Container Closure SystemsOmanAug 25PBPacific BridgeCan Foreign Clinical Data be Used to Get Your Medical Device Approved in Japan?OmanTurn Oman research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 Oman work.
Oman market-launch workpaper
Connect the Ministry of Health route, evidence, labels, local role, timing, and dependencies to a wider launch plan.
Oman dossier reuse and delta
Compare an existing authorization and evidence set against Ministry of Health administrative, testing, labeling, and dossier needs.
Oman change notification workpaper
Map a product or manufacturing change to Ministry of Health evidence, notification, timing, and implementation questions.
Oman regulatory change impact
Assess a current Ministry of Health update against one product and turn it into an owner-ready action workpaper.
Oman cybersecurity evidence review
Review connected-device architecture, risks, SBOM, testing, lifecycle controls, and market-specific questions for Oman (Ministry of Health).
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