16 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Praxiject 0.9% NaCl
FDA 510(k)
FDA Class 2
·General Hospital
NA
FDA UDI
KEY SURGICAL, INC.·10849771048920·K-Wires, Double trocar, .062-inch (1.6mm) diame...
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704292565·
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·14026704912329·
mahe medical GmbH
FDA UDI
mahe medical gmbh·04050659484108·K-Wire w. double end trocarpoint _x000D_...
K-Wire w. double end trocarpoint 1.60mm/127mm, 6 pcs./unit
FDA UDI
mahe medical gmbh·EMAHKM711090·K-Wire w. double end trocarpoint
1.60mm...
Cranial Fusion
FDA UDI
Life Spine, Inc.·00190837085278·
VIVATRAK
FDA 510(k)
FDA Class 1
·General Hospital
SACS EEG WORKSTATION A7
FDA 510(k)
FDA Class 2
·Neurology
XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NIQ·June 14, 2013
DUROM US ACETABULAR COMPONENT 48/42 H
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·July 8, 2011
LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM 9.75CM
FDA Adverse Event
Injury
·BIOENTERICS CORPORATION·Product code LTI·September 18, 2008
PERFORMER INTRODUCER
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·April 15, 2022
BD MICROLANCE¿ HYPODERMIC NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMI·November 18, 2019
PERFORMER INTRODUCER
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·September 11, 2024
PERFORMER RADIAL ACCESS SET
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·July 15, 2022