10 results
·
21ms
·
Sources: EU EUDAMED, US FDA
NEEDLE-SHIELD
FDA 510(k)
FDA Class 2
·General Hospital
TERUMO SURSHIELD- PUR SAFETY I.V. CATHETER
FDA 510(k)
FDA Class 2
·General Hospital
QMS LIDOCAINE
FDA 510(k)
FDA Class 2
·Clinical Toxicology
DERMABOND ADVANCED TOPICAL SKIN ADHESIVE
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code MPN·June 27, 2014
OMNIFIT SER. II INSERT -10 DEG.
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS CORK·Product code LPH·November 10, 2010
ACTIVE KNEE
FDA Adverse Event
ADVANCED SURGICAL DESIGN AND MANUFACTURE·Product code JWH·December 19, 2012
TO GORE-TEX® STRETCH VASCULAR GRAFT
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code DSY·July 27, 2021
GORE-TEX® STRETCH VASCULAR GRAFT
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code DSY·July 27, 2021
SURSHIELD PUR SAFETY I.V. CATHETER
FDA Adverse Event
Injury
·TERUMO CORPORATION - KOFU·Product code FOZ·December 22, 2017
GORE-TEX® STRETCH VASCULAR GRAFT
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code DSY·July 27, 2021