27 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FLAVORED MALE LATEX CONDOM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040015322·Zirlux 16+ D3 85x40x22
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040005156·Maxitest Biological Monitor
PULSE GEN MODEL UNK
FDA Adverse Event
Injury
·CYBERONICS·Product code LYJ·February 16, 2012
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K0112230·Tap, 5.50mm, Cannulated, Fixed Sleeve
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033254448·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033254530·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033254479·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033254431·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033254516·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033254462·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033254509·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033254486·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033254523·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033254493·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033254455·
ANGIO FLOW THERMODILUTION CATHETER, MODEL AF-CATH-01; ANGIOFLOW METER, MODELS HQ100 AND HQ101
FDA 510(k)
FDA Class 2
·Cardiovascular
SURGITRON IEC II
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SYNCHRON LX 20 PRO CLINICAL SYSTEMS
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·June 8, 2011
ACCU-CHEK ® AVIVA PLUS TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·March 19, 2013