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PROGAV 2.0

Aesculap AG · Model FX616T · UDI-DI 04041906502911

JXG Prescription
10
510(k) clearances
25,592
Adverse events (226 deaths)
0
Recalls
70
Facilities

Description

PROGAV 2.0 SYS SA2.0 20 & BURRHOLE RES.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.