Pro Guide

Import Medical Equipment Morocco: DMP Guide 2026

Healthcare sector in Morocco is transforming in 2026. Complete guide on AMMPS registration, device classification, and customs procedures.

Equipe Casa Horizon

Transitaire agréé

January 7, 2026

Sommaire

Historic Transformation of the Health Sector

The healthcare sector in Morocco is undergoing a historic transformation in 2026. With generalized social protection and massive hospital upgrades, demand for medical devices (MD) is peaking. However, importing a scanner or sterile consumables is a strategic operation under Law 84-12.

In 2026, the sole authority is no longer DMP but the Moroccan Agency for Medicine and Health Products (AMMPS). This guide details registration procedures, technical standards, and customs specifics to succeed in your medical import.

🏥 AMMPS: The New Medical Device Watchdog

2026 marks the full sovereignty of AMMPS, replacing DMP with increased resources.

Digitalization: Requests via PortNet interconnected platform.
Controls: Own labs to verify compliance (implants, IVD).
Delays: Target 6 months for final certificate (if perfect file).

Agrandir 🔍

📊 Device Classification (Risks)

In Morocco, as in Europe, devices are classified by risk. Higher class means stricter AMMPS clinical evidence requirements.

Risk Classes

Class I (Low)

Bandages, glasses, reusable instruments.

Class IIa (Moderate)

Lenses, ultrasound, dental crowns.

Class IIb (High)

X-ray, ventilators, lens solutions.

Class III (Critical)

Stents, breast implants, cardio catheters.

🏢 Step 1: Importer Establishment Approval

Before registering, your company must be approved as a Medical Device Establishment.

2026 Requirements

Technical Director

Pharmacist or Biomedical Engineer registered with order.

BPSD Premises

Warehouse respecting Good Practices (Temperature, Hygiene).

Quality System

Product recall procedure (Materiovigilance).

📜 Step 2: Registration Certificate

Essential for customs. Each model needs its own certificate (valid 5 years).

Technical File

AMMPS requires international standards: ISO 13485 (Manufacturer Quality), CE Mark (or FDA), and Free Sale Certificate (FSC) from origin.

🔧 Maintenance & After-Sales Obligation

Frequent blocker: Import prohibited if after-sales is not guaranteed. Must prove technical workshop, spare parts availability (5 yrs min), and team training.

💰 Customs Clearance: Taxes & Fiscal Advantages

Medical equipment enjoys preferential regime. VAT 10% on most MDs. 0% Import Duty if origin Europe or USA.

Morocco Customs Duty Simulator

Estimate the real landed cost of your import (DDP)

1Import Data

Product Value (FOB)

MAD

Shipping Cost (Freight)

Insurance (or 0)

Import Duty Rate

Standard rate (Furniture, Auto parts...).

2Simulation Results

Enter the value of your goods to see the tax breakdown.

♻️ Refurbished: Warning!

Used 'as is' is BANNED. Only factory refurbished (under 5 years, like-new warranty) is allowed for heavy equipment (MRI, Scanners).

🚑 Medical Logistics

Cold Chain

GPS Thermal containers mandatory for reagents/implants.

Fragility

Anti-vibration packaging for optics/lasers.

💡 Conclusion

Importing medical equipment to Morocco in 2026 is a responsibility. AMMPS tightening ensures patient safety. Success key: meticulous prep and expert logistics partner.

Working with Casa Horizon ensures smooth medical flow management, from port to hospital.

Frequently Asked Questions

Can I import without CE?

Yes if equivalent (FDA) and AMMPS tests, but CE makes it easier.

Class III reg time?

9 to 12 months for implantable (complex).

Spare parts registration?

No if specific to registered model and listed.

Samples?

Yes under Temporary Admission, sale prohibited.

Biomedical Engineer Role?

Technical guarantor, validates compliance and supervises service.

Sources & Références

Let's Optimize Your Supply Chain

Discuss your logistics challenges with a trade expert.

Request a Quote Switchboard