13 results
·
17ms
·
Sources: EU EUDAMED, US FDA
PROSPECT(TM) GIARDIA MICROTITER ASSAY/MODIFICATION
FDA 510(k)
FDA Class 2
·Microbiology
36M - Class B 21 White Cap - 36 Metal
FDA UDI
Certified Safety Manufacturing, Inc.·00766588220109·36M - Class B 21 White Cap - 36 Metal
36M - Class B 21 White Cap - Metal
FDA UDI
Certified Safety Manufacturing, Inc.·00766588620107·36M - Class B 21 White Cap - Metal
Precision MIS Bunion System
FDA UDI
Paragon 28, Inc.·00889795153210·K-wire, 2.0mm x 100mm
Sapphire ULTRA Coronary Dilatation Catheter
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955979200·
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K1220100·Breaker, Extended Tab
Instrument Case
FDA UDI
KATENA PRODUCTS, INC.·00841668111024·INSTRUMENT CADDY MEDIUM
TOTAL KNEE FEMORAL COMPONENT
FDA 510(k)
FDA Class 2
·Orthopedic
Z6 DIAGNOSTIC ULTRASOUND SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
SPRINT QUATTRO SECURE
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 13, 2010
HUT EXT DR FINAL ASSY-STANDARD
FDA Adverse Event
Malfunction
·LIEBEL-FLARSHEIM CO.·Product code IXR·January 15, 2013
INSIGNIA
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 9, 2014
BIOMET TIBIAL LOCKING BAR
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HRY·May 15, 2018