إجراء مقترح من ماليزيا: أدوات وأجهزة للبصريات أو للتصوير الفوتوغرافي أو السينمائي…

Following the approval of the draft Customs (Prohibition of Imports) (Amendment) (No. xx) Order 2026, the importation of medical device goods listed in Part I of the Third Schedule of P.U.(A) 117/2023 is subject to an approval letter issued by the Medical Device Authority (MDA) as the Point of Issuance Authority (PIA) for the regulated HS Codes, except for medical devices imported for personal use. Authorization to import medical devices under the Medical Device Act 2012 [Act 737] must be obtained before applying for permission to import medical devices under the Customs (Prohibition of Imports) (Amendment) (No. xx) Order 2026. The proposed amendments to the Schedules of the Customs (Prohibition of Imports) 2023 [P.U.(A) 117/2923] are as set out in the Attachment.