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: Medical devices are regulated by the Central Administration for Pharmaceutical Affairs (CAPA), part of the Egyptian Drug Authority (EDA).
Egypt has adopted the European Risk Classification System for medical devices (Class I, IIa, IIb, III and IV).
The timeframe for the registration process is six months.
Licenses issued in Egypt are valid for ten years.
An authorized representative is required.
Last updated on March 17 2015.
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