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STERILMED, INC. · Model MIC1597 · UDI-DI 10888551001748

NON Prescription
1
510(k) clearances
47
Adverse events
1
Recalls
2
Facilities

Description

BIOPSY FORCEPS LARGE CAPACITY W/NEEDLE RADIAL JAW 3 YELLOW 2.8MM MINIMUM WORKING CHANNEL

Recalls

DateFirmReason
2008-08-08Sterilmed IncSteriMed, Inc is conducting a product removal of a small group of devices individually packaged and sealed within a pouch. The removal is being conducted because the possibility e

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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.