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Devices
Device Recall Introducer guide
Model / Serial
Lot # L0104244
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Distributed in FL, OK, SC, and KS in the US. Internationaly to South Africa and the Netherlands.
Product Description
Vistabritetip IG Introducer, Introducer Guide. Labeled as sterile, sterilized with ethylene oxide gas. For single use only. Catalog number 4038553S
Manufacturer
Cordis Corporation
1 Event
Recall of Device Recall Introducer guide
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Manufacturer
Cordis Corporation
Manufacturer Address
Cordis Corporation, 14201 NW 60th Ave, Miami Lakes FL 33014-2802
Manufacturer Parent Company (2017)
Cardinal Health
Source
USFDA
Language
English
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