14 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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LAPAROSCOPIC KNITTER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·14026704921932·
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704286892·VERTEBRA SPREADER #1 WITH RATCHET (CLOWARD)
MEDCOMP PERITONEAL DIALYSIS CATHETERS
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
INTEGRAL III BIOINTEGRATED DENTAL IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
PATHROMTIN SL
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GFO·August 11, 2017
PATHROMTIN SL
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GFO·August 11, 2017
TAPERLOC POR FMRL LAT 10X140
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·November 13, 2018
M2A-MAGNUM 42-50MM TPR INSRT-6
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·November 13, 2018
PATHROMTIN SL (RILIBAK)
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GFO·January 4, 2023
REVEAL XT
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code DSI·February 11, 2013
TENDRIL SDX
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·January 10, 2011
RENEGADE? STC 18
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - CORK·Product code DQO·July 24, 2014
M2A-MAGNUM PF CUP 54ODX48ID
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·November 13, 2018