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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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258 records meeting your search criteria returned- Product Code: DQO Product Problem: Break Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
BOSTON SCIENTIFIC CORPORATION RENEGADE STC 18 09/05/2019
MEDICAL COMPONENTS INC. Long Term CVC 09/04/2019
TERUMO CORPORATION, ASHITAKA PROGREAT CATHETER 08/26/2019
TERUMO CORPORATION, ASHITAKA PROGREAT CATHETER 08/26/2019
BOSTON SCIENTIFIC CORPORATION RENEGADE STC 18 08/15/2019
MICROVENTION, INC HEADWAY DUO MICROCATHETER 06/28/2019
MERIT MEDICAL SYSTEMS, INC. IMPRESS DIAGNOSTIC CATHETER 05/03/2019
MERIT MEDICAL SYSTEMS, INC. IMPRESS PERIPHERAL CATHETER 04/09/2019
MERIT MEDICAL SYSTEMS, INC. IMPRESS PERIPHERAL CATHETER 04/09/2019
STRYKER NEUROVASCULAR-UTAH-SALT LAKE CIT TREVO PRO 18RO MICROCATHETER 02/19/2019
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