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Probe And Director, Gastro-Urology

FDA product code FGM · Class 1 · Gastroenterology, Urology

307
Registered devices
20
Adverse events
1
Recalls
7
510(k) clearances

Devices with this code

Millennium — Avalign Technologies, Inc.RZ Medizintechnik GmbH — RZ-Medizintechnik GmbHMillennium — Avalign Technologies, Inc.Integra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONIntegra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONAESCULAP — Aesculap AGIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONRZ Medizintechnik GmbH — RZ-Medizintechnik GmbHV. Mueller — STERIS CORPORATIONV. Mueller — STERIS CORPORATIONAESCULAP — AESCULAP, INC.Grooved Director — SONTEC INSTRUMENTS, INC.BEAR — Bear-Ent, LLCHNM Medical — HNM STAINLESS, LLC.Integra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONLARRY FISTULA PROBE — SONTEC INSTRUMENTS, INC.Integra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONIntegra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONMedicon — Medicon eG. Chirurgiemechaniker-GenossenschaftV. Mueller — STERIS CORPORATION

Recent recalls

DateFirmReason
2004-02-06Medtronic Gastroenterology / UrologyThe product's rear panel label could smear during use causing the serial number to be unreadible. This has the remote possibility of resulting in patient data

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