24 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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INTERCEPT ORAL FLUID DRUG TEST ORAL SPECIMEN COLLECTION DEVICE, MODEL 503-XXXX
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040013328·Zirlux 16+ D3 98.5X12
Beaver Visitec Inter
FDA UDI
GRI Medical & Electronic Technology Co., Ltd.·16931918134024·Adhesive Incise Film_20 x 10 cm_Non-sterile_300...
NVM5
FDA UDI
Nuvasive, Inc.·00887517163271·NVJJB Dual Electrode Imped Meter Leads
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033220580·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033220597·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033220627·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033220573·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033220641·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033220634·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033220566·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033220610·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033220603·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033221884·
AGILENT INFORMATION CENTER SOFTWARE FOR M3150A AND M3153A AND AGILENT M2/M3/M4 COMPACT PORTABLE PATIENT MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
MODIFICATION TO ARTOSCAN M
FDA 510(k)
FDA Class 2
·Radiology
BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM
FDA Adverse Event
Malfunction
·BD (SUZHOU)·Product code FOZ·October 13, 2022
VERTEBRAL SPACER-TR 10MMX27MM 11MM HEIGHT
FDA Adverse Event
Malfunction
·SYNTHES ELMIRA·Product code MQP·February 20, 2013
7900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·March 14, 2013
M2A MAGNUM PF CUP 58MM OD X 52MM ID
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·March 8, 2011