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TREWAVIS SURGICAL

TREWAVIS SURGICAL INSTRUMENTS PTY LTD · Model SBT100 · UDI-DI 09340254000632

FCK
1
510(k) clearances
17
Adverse events
1
Recalls
4
Facilities

Description

MODEL TR RECTAL SUCTION BIOPSY TUBE (INSTRUMENT, BIOPSY, SUCTION) (Rectal Suction Biopsy Tool)

Recalls

DateFirmReason
2011-11-03Bard Peripheral Vascular IncThis recall was voluntarily initiated by the firm due to the product 's damaged packaging trays; cracked EnCor (Trademark) packaging trays, plastic PETG tray the probe is packaged

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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.