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Gimmi

Gimmi GmbH · Model T.9635.00 · UDI-DI 04049047109099

EZO Prescription
5
510(k) clearances
69
Adverse events
1
Recalls
37
Facilities

Description

URETHROTOME SHEATH 21 CH, CHANNEL 5 CH , FOR 0° SCOPES FOR FILIFORMBOUGIES OR CATHETERS

Recalls

DateFirmReason
2010-12-22Olympus America Inc.The device sterile package seal shows evidence of being breached or was breached

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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.