The Arabian Stories, 20 April 2026: The Ministry of Health has announced that medical device companies must comply with new certification and registration requirements within six months, warning that non‑compliant shipments will be suspended.

Oman’s Ministry of Health issued a directive requiring medical device manufacturers and importers to regularise their status under the country’s updated regulatory framework.

Key provisions include:

• Deadline: Six months from 22 April 2026 to complete certification and registration.
• Scope: Applies to all medical devices imported into Oman, including diagnostic, therapeutic, and surgical equipment.
• Enforcement: Shipments from non‑compliant firms will be suspended at entry points.
• Legal basis: Regulations issued under the law and executive decisions of the Ministry of Health.

The Ministry emphasised that the measure is designed to strengthen patient safety, ensure product quality, and align Oman’s medical device market with international standards. Importers were reminded that the government will not assume responsibility for contractual or financial losses arising from non‑compliance.

For more news and content, try Lexis Middle East. Click on lexis.ae/demo to begin your free trial of Lexis® Middle East platform.

You can also explore the legal landscape by subscribing to our Weekly Newsletter.

Want to learn more about Lexis® Middle East? Visit https://www.lexis.ae/lexis-middle-east-law/.