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IT MOH: Difference between revisions

From Teltonika Telemedic Wiki
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<div style="background: linear-gradient(135deg, #1a1a1a 0%, #2d2d2d 50%, #3a3a3a 100%); border-radius: 12px; padding: 36px 40px; margin-bottom: 28px; box-shadow: 0 4px 24px rgba(0,0,0,0.18);">
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<td style="vertical-align: middle; padding-right: 20px; width: 96px; background: #ffffff; border-radius: 8px;"><div style="text-align: center; padding-left: 6px;">[[File:Italy_MOH_logo.png|alt=UKCA logo.|center|frameless|80x80px]]</div></td>
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<div style="font-size: 28px; font-weight: 700; color: #ffffff; letter-spacing: -0.5px; margin-bottom: 8px;">Italy MOH — BD/RDM Registration</div>
<div style="font-size: 28px; font-weight: 700; color: #ffffff; letter-spacing: -0.5px; margin-bottom: 8px;">Italy MOH — BD/RDM Registration</div>
<div style="color: #c4c4c4; font-size: 15px; line-height: 1.6;">Registration in the Italian Ministry of Health's Banca Dati / Repertorio Dispositivi Medici (BD/RDM) is required for medical devices placed on the Italian market under Regulation (EU) 2017/745 (MDR).</div>
<div style="color: #c4c4c4; font-size: 15px; line-height: 1.6;">Registration in the Italian Ministry of Health's Banca Dati / Repertorio Dispositivi Medici (BD/RDM) is required for medical devices placed on the Italian market under Regulation (EU) 2017/745 (MDR).</div>
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Latest revision as of 13:46, 7 July 2026

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