10 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Altaviz Needle Kit
FDA 510(k)
FDA Class 2
·General Hospital
BD Difco™ Salmonella H Antiserum Spicer-Edwards 4
FDA UDI
BECTON, DICKINSON AND COMPANY·00382902226819·BD Difco™ Salmonella H Antiserum Spicer-Edwards...
AZOG, INC. HCG ONE-STEP URINE PREGNANCY TEST (DEVICE OR CASSETTE)
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Promisemed Covered Safety Pen Needle
FDA 510(k)
FDA Class 2
·General Hospital
FREESTYLE LIBRE
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC·Product code PZE·November 23, 2021
BD VACUTAINER® BUFFERED SODIUM CITRATE (9NC) BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·January 18, 2024
TAXUS (R) LIBERTÉ (R)
FDA Adverse Event
Death
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·August 25, 2011
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·November 4, 2014
EXTRACTOR? PRO RX
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - CORK·Product code FGE·July 12, 2013
SpF PLUS-Mini (60 ¿A/W) Implantable Spinal Fusion Stimulator SpF PLUS-Mini Implantable Fusion Stimulators are indicated as a spinal fusion adjunct to increase the probability of fusion success in 1 or 2 levels
FDA Enforcement
Class I
·Terminated·Zimmer Biomet, Inc.·November 7, 2018