3 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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PediaLift
FDA UDI
PEDIALIFT LLC·B751PDLFT0·PediaLift Crib Infant Access Device
PediaLift Access Device, Device Identifier: B751PDLFT0
FDA Recall
Terminated
·PediaLift LLC·Product code FMS·July 3, 2019
PediaLift Access Device, Device Identifier: B751PDLFT0
FDA Enforcement
Class II
·Terminated·PediaLift LLC·February 12, 2020