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Transtrack Patient Roller 67

MIZUHO ORTHOPEDIC SYSTEMS, INC. · Model 900 · UDI-DI 00842430107412

FMR
5
510(k) clearances
132
Adverse events (2 deaths)
0
Recalls
248
Facilities

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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.