11 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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KIDNEYvault Portable Renal Perfusion System
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
LANDMARK REBOA Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
DISPOSABLE POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVES, WHITE COLOR (SENSI-PRO)
FDA 510(k)
FDA Class 1
·General Hospital
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·September 13, 2024
TBL PACKAGE, VERITER 5TH WHEEL SIDNE ENABLED ASSY
FDA Adverse Event
Malfunction
·STRYKER COMMUNICATIONS·Product code FQO·November 4, 2008
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code MDS·August 29, 2011
ACCU-CHEK ® MOBILE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·July 18, 2013
AnchorFast Guard Select, Oral Endotracheal Tube Fastener, REF 9700,
FDA Recall
Open, Classified
·Hollister Incorporated·Product code CBH·December 23, 2024
AnchorFast, Oral Endotracheal Tube Fastener, REF 9799,
FDA Recall
Open, Classified
·Hollister Incorporated·Product code CBH·December 23, 2024
AnchorFast SlimFit, Oral Endotracheal Tube Fastener, REF 9787,
FDA Recall
Open, Classified
·Hollister Incorporated·Product code CBH·December 23, 2024
AnchorFast Guard, Oral Endotracheal Tube Fastener, REF 9800,
FDA Recall
Open, Classified
·Hollister Incorporated·Product code CBH·December 23, 2024