21 results
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36ms
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Sources: EU EUDAMED, US FDA
MULTI-DAY ELECTRODES
FDA 510(k)
FDA Class 2
·Neurology
K2-HF OPAQUER powder, O-C1, 20g.
FDA UDI
Yeti Dentalprodukte GmbH·EYET38620110·
Shoreline™ ACS
FDA UDI
Seaspine Orthopedics Corporation·10889981177362·Modular Trial, 20 x 15 x 11mm, 7 Deg Lordosis
Symmetry Iris
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482128039·Symmetry® Scissors, Iris, Straight, Serrated, B...
MedDream
FDA 510(k)
FDA Class 2
·Radiology
MODIFICATION TO FLOWSCREEN
FDA 510(k)
FDA Class 2
·Anesthesiology
VerSys®
FDA UDI
Zimmer, Inc.·00889024173255·
VerSys®
FDA UDI
Zimmer, Inc.·00889024173248·
VerSys®
FDA UDI
Zimmer, Inc.·00889024138827·
VerSys®
FDA UDI
Zimmer, Inc.·00889024138810·
VerSys®
FDA UDI
Zimmer, Inc.·00889024366763·
VerSys®
FDA UDI
Zimmer, Inc.·00889024173262·
VerSys®
FDA UDI
Zimmer, Inc.·00889024138803·
VerSys®
FDA UDI
Zimmer, Inc.·00889024138797·
FEMORAL HEAD 12/14 TAPER
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code LPH·March 17, 2020
SCREW,FIXATION,BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·May 18, 2015
SPECTTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 23, 2014
INTEGRATED APD SET W/CASSETTE3-PRONG
FDA Adverse Event
BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·October 8, 2010
IN TOUCH ZU
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·October 31, 2012
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·July 27, 2015