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MDR: end of transition for class III and implantable IIb

European CommissionCompliance deadline High impact in 412 days
Date
Fri 31 Dec 2027
Body
European Commission
Scope
EU
Subject
Medical devices
Official source
eur-lex.europa.eu

Last day legacy class III devices and most class IIb implantable devices can be placed on the market under the extended MDR transition, provided the 2024 application/agreement conditions were met. MDR certification must be in place after this.

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Dates are taken from the official source above. Agencies occasionally reschedule; confirm on the source before acting.