53 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BD ECLIPSE HYPODERMIC NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
30 G X 1/2 IN. BD ECLIPSE¿ 1 ML BD LUER-LOK¿ SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FMI·February 7, 2019
25 G X 5/8 IN. BD ECLIPSE¿ NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMI·March 1, 2016
27 G X 1/2 IN. BD ECLIPSE¿ 1 ML BD LUER-LOK¿ SYRINGE WITH DETACHABLE NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FMI·November 30, 2016
25 G X 5/8 IN. BD ECLIPSE¿ 1 ML BD LUER-LOK¿ SYRINGE WITH DETACHABLE NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FMI·February 24, 2017
27 G X 1/2 IN. BD ECLIPSE¿ 1 ML BD LUER-LOK¿ SYRINGE WITH DETACHABLE NEEDLE
FDA Adverse Event
Injury
·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FMI·November 30, 2016
Vivid Nano Flow Refill Syringe Opaque
FDA UDI
PEARSON DENTAL SUPPLIES, INC.·D724D0101880·
CARDINAL HEALTH
FDA UDI
Cardinal Health 200, LLC·10887488094120·IV START
QUIK-COMBO PACING/DEFIBRILLATION/ECG ELECTRODES
FDA Adverse Event
Malfunction
·MEDTRONIC PHYSIO-CONTROL CORP.·Product code MLN·September 26, 2000
FAST-PATCH PLUS DISPOSABLE DEFIBRILLATION/ECG ELECTRODES WIT
FDA Adverse Event
Malfunction
·MEDTRONIC PHYSIO-CONTROL CORP.·Product code MLN·September 26, 2000
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033106907·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033106914·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033106884·
InTess Lumbar Cage
FDA UDI
Kalitec Direct LLC·B07312K0101080·Distractor, Smooth Paddle, 8mm
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033106891·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033106921·
TiWAVE L Lumbar Cage System
FDA UDI
Kalitec Direct LLC·B07323K0101080·Distractor, Smooth Paddle, Lordotic, 8mm
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033106938·
GLEN RESURFACING REAMER D27 MM
FDA Adverse Event
Malfunction
·DEPUY FRANCE SAS REG. # 3003895575·Product code LXH·December 26, 2013
REAL PATIENT AMBULATORY EEG, MODEL EX-AMB-RP (PROPOSED)
FDA 510(k)
FDA Class 2
·Neurology