500 results
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43ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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GenePOC GBS LB
FDA 510(k)
FDA Class 1
·Microbiology
SOLITARIE PEEK ANTERIOR SPINAL SYSTEM-TO BE CALLED COLITAIRE 35
FDA 510(k)
FDA Class 2
·Orthopedic
MP 719
FDA 510(k)
FDA Unclassified
·Unknown
BIODESIGN URETHRAL SLING
FDA Adverse Event
Injury
·COOK BIOTECH, INC.·Product code PAG·October 9, 2014
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 21, 2011
SENOMARK BREAST BIOPSY MARKER
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code NEU·May 28, 2013
Phoenix AP AST Indicator Bag, Catalog Number 246006
FDA Enforcement
Class II
·Terminated·Becton Dickinson & Co.·March 6, 2019
GUNTHER TULIP NAVALIGN FEMORAL VENA CAVA FILTER SET
FDA Adverse Event
Death
·WILLIAM COOK EUROPE·Product code DTK·July 23, 2019
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·July 9, 2020
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·October 2, 2019
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·October 31, 2019
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·October 7, 2019
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·October 7, 2019
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·October 2, 2019
(17-0557) ANK C/X IMPL B17/D4.5/L17(IMPLANTS)
FDA Adverse Event
Injury
·DENTSPLY IMPLANTS (A DIVISION OF DENTSPLY IH AB)·Product code DZE·June 17, 2021
GUNTHER TULIP NAVALIGN JUGULAR VENA CAVA FILTER SET
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·February 5, 2021
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·December 5, 2019
AUTOPULSE® LIFEBAND
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION·Product code DRM·February 4, 2022
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·September 9, 2020
UNKNOWN
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·April 21, 2020