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MiniMed™ Mobile

MEDTRONIC MINIMED, INC. · Model MMT-6103 · UDI-DI 00763000480660

PKU
0
510(k) clearances
38,004
Adverse events
0
Recalls
7
Facilities

Description

SFTWR MMT-6103 MM MBL CLIN ANDRD 1.0.0

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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.