FDA clears Penumbra's Red 62 reperfusion catheter for removing brain blood clots

Retrieved on: 2021-06-23 15:56:15

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FDA clears Penumbra's Red 62 reperfusion catheter for removing brain blood clots. View article details on hiswai:

Excerpt

UDI labeling can identify medical devices through their distribution and use. The deadline for labeling Class 1 and unclassified devices is coming up.

Article found on: www.massdevice.com

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