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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall Materialise Distributed by Biomet Orthopedics, Signature Personalized Patient Care System Orthopedic Devices Materialise N.V. 2 United States USFDA
Device Recall Signature Personalized Patient Care System Orthopedic Devices Materialise USA LLC 2 United States USFDA
Device Recall LPSFlex Pin Guides Orthopedic Devices Materialise USA LLC 2 United States USFDA
Device Recall NK Flex Pin Guides Orthopedic Devices Materialise USA LLC 2 United States USFDA
Device Recall Signature Orthopedic Devices Materialise USA LLC 2 United States USFDA
Zimmer Patient Specific Instrument PERSONA CR Pin Guides Orthopedic Devices Materialise USA LLC 2 United States USFDA