12 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DLP SINGLE STAGE VENOUS CANNULA, DLP RIGHT ANGLE SINGLE STAGE VENOUS CANNULA, DLP SINGLE STAGE VENOUS CANNULA WITH RIGHT
FDA 510(k)
FDA Class 2
·Cardiovascular
Hayden Medical
FDA UDI
Hayden Medical, Inc.·00840319704264·Barraquer (Kurth) Cilia & Suture Forceps 4-1/2"...
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450192955·
HUMAPEN LUXURA HD
FDA 510(k)
FDA Class 2
·General Hospital
PAIN CARE 4200
FDA 510(k)
FDA Class 2
·General Hospital
BD VACUTAINER® SST¿ II ADVANCE PLUS BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·August 30, 2018
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·May 16, 2025
NV GXL LINR, NTRL, 36MM ID, GROUP 4 CUPS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code LZO·January 2, 2024
SENSOR BSA
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code MDS·May 20, 2013
ECHELON*FLEX60 ARTICULATING
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 13, 2011
CONTOUR TEST STRIPS (50)
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE, LLC·Product code NBW·August 13, 2008
Stolen McGRATH MAC Video Laryngoscopes, REF: 301-000-000
FDA Enforcement
Class I
·Ongoing·Covidien·November 8, 2023