16 Feb Regulatory Process for Magnetic Resonance Imaging (MRI) Equipment
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This communication is intended to guide relevant industries on the regulatory process for Magnetic Resonance Imaging (MRI) equipment. MRI equipment falls within the definition of electronic products and is classified as Group III under the Hazardous Substances Act 15 of 1973. MRIs are also listed in Section 5, Regulation 1302 of the Schedule of Listed Electronic Products.
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Document Number:
RDN02-2025/26
Version:
1
Date Updated:
16/02/2026
File Type:
www
Category:
Communication to industry