19 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MONOPOLAR CURVED SCISSORS TIP COVER ACCESSORY
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
n/a
FDA UDI
HANS RUDOLPH, INC.·00874750006205·2700B 2WAY T SHP W/BODY SALIVA
CASPIAN Spinal System
FDA UDI
VB Spine LLC·10888857235533·Connector Assembly Tube
MARQUETTE EAGLE MONITOR MODEL 4000, MODEL N3024
FDA 510(k)
FDA Class 2
·Cardiovascular
HORIZON PERINATAL CARE SURVEILLANCE AND ARCHIVAL MODEL VERSON 4.0
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·July 31, 2014
TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·July 31, 2014
CLINICAL CHEMISTRY MAGNESIUM
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING INC·Product code JGJ·May 14, 2013
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·August 15, 2008
PROXIMATE** RH ROTATING HEAD SKIN STAPLER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDT·June 3, 2011
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·February 28, 2022
TRIFORCE¿ PERIPHERAL CROSSING SET
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·August 1, 2015
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·April 1, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·April 1, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·August 8, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·July 2, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·May 2, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·PFIZER, INC.·Product code QJR·May 8, 2023
INLIVEN CRT-P, Model Numbers: a) V284 b) V285 c) W274 d) W275 (added 7/15/2021)
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·July 21, 2021