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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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212 records meeting your search criteria returned- Product Code: DQO Product Problem: Detachment Of Device Component Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
ARROW INTERNATIONAL ARROW RADIAL ARTERY CATHEERIZATION SET 07/07/2017
CORDIS CORPORATION CATH MB 5F PIG 110CM 6SH 06/19/2017
TERUMO CORPORATION, ASHITAKA RADIFOCUS GLIDECATH 05/31/2017
CORDIS CORPORATION UNKNOWN TRAPEASE VENA CAVA FILTER 05/25/2017
ABIOMED ABIOMED 05/25/2017
CORDIS DE MEXICO CATH TEMPO AQUA 4F C2 65CM 05/22/2017
CORDIS DE MEXICO CATH MB 5F PIG 110CM 6SH SUPERTORQUE MAR 05/12/2017
CORDIS DE MEXICO CATH MB 5F PIG 110CM 6SH 05/11/2017
CORDIS DE MEXICO CATH F6 INF TL JL 3.5 100 CM 05/04/2017
CORDIS DE MEXICO CATH TEMPO 4F UF 65CM 5SH 04/21/2017
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