29 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CENTRASIL SILICONE ELASTOMER CENTRAL VENOUS CATH
FDA 510(k)
FDA Class 2
·General Hospital
Archon
FDA UDI
Nuvasive, Inc.·00887517309631·Archon Screw, 4.0x15mm S.D. Variable
Snowden-Pencer
FDA UDI
STERIS CORPORATION·10885403151828·Snowden-Pencer RETRACTOR WEITLANIER 11.5CM 4-1/...
dentaform®
FDA UDI
DENTAURUM GmbH & Co.KG·J011881215180·dentaform® Snap Band, Tooth 36, Size 15/Roth 18
dentaform®
FDA UDI
DENTAURUM GmbH & Co.KG·J011881215000·dentaform® Snap Band, Tooth 36, Size 15
dentaform®
FDA UDI
DENTAURUM GmbH & Co.KG·J011881215220·dentaform® Snap Band, Tooth 36, Size 15/Roth 22
Infrared Thermometer
FDA 510(k)
FDA Class 2
·General Hospital
VOLUMINA
FDA 510(k)
FDA Class 2
·Radiology
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·February 12, 2016
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·February 12, 2016
TSRH
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·June 27, 2017
TSRH
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·June 27, 2017
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·October 13, 2017
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·June 3, 2019
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·October 7, 2015
TSRH
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·March 31, 2016
BIVONA TTS CUFFED PEDIATRIC TRACHEOSTOMY TUBE
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code JOH·November 14, 2012
PROLIFT PELVIC FLOOR REPAIR
FDA Adverse Event
Injury
·ETHICON, INC.·Product code FTL·October 20, 2010
GORE EXCLUDER AAA ENDOPROSTHESIS
FDA Adverse Event
Malfunction
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·February 12, 2014
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·January 11, 2012