17 results
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36ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ANGIOGRAPHIC BALLOON CATHETER BY J-LLOYD
FDA 510(k)
FDA Class 2
·Cardiovascular
BARCO
FDA UDI
Barco NV·05415334041653·MDSC-8532 SSTF
N/A
FDA UDI
Zimmer, Inc.·00889024178823·
N/A
FDA UDI
Zimmer, Inc.·00889024178847·
N/A
FDA UDI
Zimmer, Inc.·00889024178892·
N/A
FDA UDI
Zimmer, Inc.·00889024178885·
N/A
FDA UDI
Zimmer, Inc.·00889024178830·
N/A
FDA UDI
Zimmer, Inc.·00889024178861·
N/A
FDA UDI
Zimmer, Inc.·00889024178908·
N/A
FDA UDI
Zimmer, Inc.·00889024178878·
N/A
FDA UDI
Zimmer, Inc.·00889024178854·
EW-10 AND EW-20
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ANTIGENZ CHLAMYDIA
FDA 510(k)
FDA Class 2
·Neurology
UNKNOWN LINER
FDA Adverse Event
Injury
·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code JDL·December 22, 2022
HEARTMATE II SYSTEM CONTROLLER
FDA Adverse Event
Malfunction
·THORATEC CORPORATION·Product code DSQ·November 17, 2010
ZYNEX
FDA Adverse Event
Other
·ZYNEX MEDICAL INC.·Product code GZJ·January 23, 2013
ACCU-CHEK ® COMPACT TEST DRUM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·July 15, 2014