15 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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C100 WRINKLE REDUCTION DEVICE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613017729·K-Wire, Double Ended, Trocar Point, Diameter Si...
B.BRAUN
FDA UDI
B. BRAUN MEDICAL INC.·04046964232152·EVA Gravity Mixing Container, 2-lead Vented Tr...
Sheehy HA/C Polycel® P.O.P.
FDA UDI
MEDTRONIC XOMED, INC.·00763000034832·PROSTHESIS 1112362 SHEEHY POP H/A POLYCL
Sheehy
FDA UDI
MEDTRONIC XOMED, INC.·00681490033664·PROSTHESIS 1112362 SHEEHY POP H/A POLYCL
POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)
FDA 510(k)
FDA Class 1
·General Hospital
MODIFICATION TO VASCULAR CLOSURE DEVICE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PEN NDL 29GA 12.7MM 100 BX 1200 USA
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND CO.·Product code FMI·March 19, 2021
HFN RH 130 DEG 9MM X 360MM
FDA Adverse Event
Injury
·BIOMET TRAUMA·Product code HSB·May 14, 2013
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 24, 2014
HIRES 90K
FDA Adverse Event
Injury
·ADVANCED BIONICS, LLC·Product code MCM·May 25, 2011
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·May 2, 2022
FLEXI SEAL SIGNAL (FMS)
FDA Adverse Event
Injury
·CONVATEC INC.·Product code KNT·October 11, 2016
CARDIOSAVE Intra-Aortic Balloon Pump An electromechanical system used to inflate and deflate intra-aortic balloons. It provide temporary support to the left ventricle via the principle of counterpulsation.
FDA Enforcement
Class II
·Terminated·Maquet Cardiovascular, LLC·January 16, 2013