Officers and regulatory representatives of ORTOPEDIFLEX DI GIUNCHI ROBERTO
RAPAGNANI ANDREA
The manufacturer currently places only legacy devices on the market under transitional provisions. PRRC designation under Article 15 MDR is not applicable at this stage. The Laa is external consultant acting for ensuring device conformity, technical documentation compliance, post-market surveillance and vigilance reporting obligations.
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Device catalog for ORTOPEDIFLEX DI GIUNCHI ROBERTO
No devices registered for this manufacturer.
Certificate health for ORTOPEDIFLEX DI GIUNCHI ROBERTO