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Mui Scientific

H & A Mui Enterprises Inc · Model CR4-1034 · UDI-DI 00678467502575

KLA
1
510(k) clearances
7
Adverse events
1
Recalls
15
Facilities

Description

16-Channel High Resolution Anorectal Catheter

Recalls

DateFirmReason
2006-04-06Medtronic Gastroenterology / UrologyMislabeling- The 8 ports of the manometric catheter were incorrectly labeled 1,3,5,7,8,2,4,6 from the distal to the proximal end of the catheter. The correct port configuration is

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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.