ADRIA SRL

2 recalls on record · Latest: Oct 27, 2021

FDA Devices Moderate Oct 27, 2021

Herniatome, 17G x 15cm, Lumbar Type, Model Number 5091745

FDA Devices Moderate Oct 27, 2021

Herniatome, 17G x 9cm, Cervical Type, Model Number 5091749

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