12 results
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44ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CDD-PCA(TM) MODEL 5800R AMBULATORY INFUSION PUMP
FDA 510(k)
FDA Class 2
·General Hospital
POWDER FREE NITRILE EXAMINATION GLOVES, VIOLET COLOR
FDA 510(k)
FDA Class 1
·General Hospital
LUMAGEM MOLECULAR BREAST IMAGING SYSTEM
FDA 510(k)
FDA Class 1
·Radiology
LEXINGTON MEM W COLUMBIA SC 2
FDA Adverse Event
Other
·SORIN GROUP USA, INC.·Product code DTZ·October 30, 2013
BD VACUTAINER® CPT¿ CELL PREPARATION TUBE WITH SODIUM HEPARIN
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·May 31, 2018
BD VACUTAINER® CPT¿ CELL PREPARATION TUBE WITH SODIUM CITRATE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·May 18, 2018
INCEPTA
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 11, 2013
OMNIPOD INSULIN PUMP
FDA Adverse Event
Injury
·INSULET CORPORATION·Product code LZG·November 24, 2010
EASYTRAK 2
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NIK·July 3, 2014
BD VACUTAINER® CPT¿ CELL PREPARATION TUBE WITH SODIUM CITRATE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·March 8, 2022
ARCHITECT C16000 SYSTEM
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING INC·Product code JJE·May 10, 2019
BD VACUTAINER® CPT¿ CELL PREPARATION TUBE WITH SODIUM CITRATE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·December 10, 2019