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MEDTRONIC MINIMED, INC. · Model MMT-6112 · UDI-DI 00763000432645
0
510(k) clearances
38,026
Adverse events
0
Recalls
7
Facilities
Description
SFTWR MMT-6112 CP IOS V2.2.0 OUS
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 docsData 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.
