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HANAROSTENT LowAxTM Duodenum/Pylorus(NNN)
M.I.Tech Co., Ltd. · Model DNJF-20-060-140 · UDI-DI 08806367076496
MUM
Prescription
1
510(k) clearances
992
Adverse events (55 deaths)
0
Recalls
13
Facilities
Description
Un-covered self-expanding nitinol Duodenum stent
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.
