25 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AMEDA HYGIENIKIT
FDA 510(k)
FDA Class 1
·Obstetrics/Gynecology
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040010440·Zirlux 16+ B2 100X18
MYELO-NATE
FDA UDI
UTAH MEDICAL PRODUCTS, INC.·H67140115190·MYELO-NATE 25 GA. 1" NDL
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033290354·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033290330·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033290361·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033290378·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033290347·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033290415·
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07310K0115100·Handle, Targeting Needle
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033290422·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033290385·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033290392·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033290439·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033290408·
BD CONNECTA¿ STOPCOCK
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMG·July 20, 2018
ACTICOAT 7 DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
MAGNUM FLOW IRRIGATION SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC.·Product code LFR·May 14, 2007
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2013