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1 PROTOCOL ON PROHIBITIONS OR RESTRICTIONS ON THE USE OF MINES, BOOBY-TRAPS AND OTHER DEVICES AS AMENDED ON 3 MAY 1996 ANNEXED TO THE CONVENTION ON PROHIBITIONS OR RESTRICTIONS ON THE USE OF CERTAIN
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The OFORMR devices form is a document used to report and track medical devices in the market.
Manufacturers and distributors of medical devices are required to file OFORMR devices forms.
The OFORMR devices form can be filled out online on the designated platform provided by the regulatory authority.
The purpose of the OFORMR devices form is to ensure the safety and effectiveness of medical devices in the market.
The OFORMR devices form requires information such as device specifications, manufacturing details, and adverse event reports.
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