FDA Device Intelligence
Home › MEDTRONIC, INC. › Tri-Ad™

Tri-Ad™

MEDTRONIC, INC. · Model 900SFC226 · UDI-DI 00763000659516

KRH Prescription
1
510(k) clearances
9,673
Adverse events (780 deaths)
0
Recalls
15
Facilities

Description

BAND 900SFC226 TRI AD 2 TRICUSPID MDR

Query this across every FDA database — by API.

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

Get your free API keyRead the docs
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.