8 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OnPoint Augmented Reality Spine System
FDA 510(k)
FDA Class 2
·Neurology
BD VACUTAINER® ECLIPSE¿ BLOOD COLLECTION NEEDLE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code FMI·November 5, 2019
N APOLIPOPROTEIN STANDARD SERUM
FDA 510(k)
FDA Class 2
·Clinical Chemistry
BREAST VOLUME NAVIGATOR
FDA 510(k)
FDA Class 2
·Radiology
LAP-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEM (SMALL) ACCESS PORT I
FDA Adverse Event
Malfunction
·COSTA RICA·Product code LTI·November 18, 2008
COLLEAGUE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 9, 2011
COULTER® LH 750 HEMATOLOGY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·July 22, 2013
BD VACUTAINER® SST¿ II ADVANCE PLUS BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·March 13, 2025