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SFDA MDS-G21

MDS-G21

Guidance on Requirements of Shipments Clearance at Ports of Entry
Saudi ArabiaSaudi Food and Drug AuthorityRegistrationEffective 2020
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What this code is

MDS-G21 is the official SFDA identifier for “Guidance on Requirements of Shipments Clearance at Ports of Entry”. MDS-G21 is the official identifier SFDA uses for this instrument.

Instrument
MDS-G21
Full name
MDS-G21
Category
Registration
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Authority source
English
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Dates
Published
20 October 2020
Effective
2020
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About this regulation

Guidance on Requirements of Shipments Clearance at Ports of Entry

MDS-G21 Version 4.0 (20 October 2020): shipment clearance requirements at the Kingdom’s ports of entry — no import without SFDA clearance, the used-device prohibition, remaining-shelf-life thresholds (40% under one year, 60% over one year), storage and data-logger obligations, sample withdrawal, the ten POEs, the per-shipment required documents (purchase invoice, bill of lading/air waybill, declaration of conformity, MDEL copy), and the clearance flowchart. Title corrected to the official cover.

MDS-G21 is the official identifier SFDA uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.

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