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ORIGIO INC. · Model MBBC018-0 · UDI-DI 20888937901034

MQH Prescription
10
510(k) clearances
27
Adverse events
4
Recalls
25
Facilities

Description

BIOPSY MICROPIPETS

Recalls

DateFirmReason
2019-03-27CooperSurgical, Inc.ICSI CUSTOM MICROPIPETTES the thirty-degree bend is absent
2008-03-02Cook Vascular Inc.mislabeled - 300 micron flexipets labeled as 130 micron and vice versa
2008-03-02Cook Vascular Inc.mislabeled - 300 micron flexipets labeled as 130 micron and vice versa
2007-12-17Cook Vascular Inc.mislabeled - 300 micron flexipets were labeled as 80 microns

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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.