26 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ETEST CEFTAROLINE
FDA 510(k)
FDA Class 2
·Microbiology
PureLife+ 5oz Plastic Cups
FDA UDI
PURELIFE, LLC·D79011210021·PureLife+ 5oz Plastic Cups, White, High-quality...
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR31210021·Ligature wire preformed open soft .010"
Baby Gorilla®/Gorilla® Plating System
FDA UDI
Paragon 28, Inc.·00889795124074·Distal Medial Tibia Plate, Large
Invictus
FDA UDI
ALPHATEC SPINE, INC.·00190376240947·AO Quick Connect Axial Handle, Fixed with Jewel...
OsteoMed
FDA UDI
OSTEOMED LLC·00845694053327·PrimaLIF LLIF Modular Angled Inserter - Left
A-PULSE CASPRO MODEL T7100, A-PULSE CASPAL MODEL T7200
FDA 510(k)
FDA Class 2
·Cardiovascular
REPROCESSED ENDOSCOPIC TROCARS
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ACCELERATOR A3600
FDA Adverse Event
Malfunction
·INPECO SA·Product code JQP·December 20, 2024
L-CATH PEEL AWAY SYSTEM
FDA Adverse Event
Injury
·LUTHER MEDICAL PRODUCTS, INC.·Product code DQO·December 5, 2002
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024468825·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024468870·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024468887·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024468863·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024468818·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024468849·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024468832·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024468856·
OT PING METER
FDA Adverse Event
Injury
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2013
HUDSON CONCHA NEPTUNE
FDA Adverse Event
Malfunction
·TELEFLEX·Product code BTT·July 28, 2014