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SenSight™

MEDTRONIC, INC. · Model B3400040M · UDI-DI 00763000426460

PJSMBXMRUNHLMHY Prescription
0
510(k) clearances
2,224
Adverse events (5 deaths)
0
Recalls
29
Facilities

Description

EXT B3400040M SENSIGHT W/MKR EMAN LJ53

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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.