30 results
·
25ms
·
Sources: EU EUDAMED, US FDA
I.V. SKY-HOOK
FDA 510(k)
FDA Class 1
·General Hospital
PAQ. 120x100x(2x150) AR1200-OEM ET MEDI
FDA UDI
AB MEDICA GROUP, S.A.·08428763008897·
Penrose Drain
FDA UDI
C. R. Bard, Inc.·00801741051234·Penrose Drain 12" (304.8mm), X-Ray Opaque Rubbe...
ENDO-SCRUB®
FDA UDI
MEDTRONIC XOMED, INC.·20681490050887·SHEATH 1912010 5PK 4MM/30DEG STORZ XOMED
Reprocessed 4mm EndoScrub Sheath, 30 deg
FDA UDI
SURETEK MEDICAL·B39019120101·
PROFYLE
FDA UDI
Stryker GmbH·07613153152156·Modular Sterilizing Container
PROFYLE
FDA UDI
Stryker GmbH·34546540244261·BONE SCREWS, CROSS-FIT, SELF-TAPPING
AEROCHAMBER PLUS FLOW-VU ANTI-STATIC VALVED HOLDING CHAMBER (VHC)
FDA 510(k)
FDA Class 2
·Anesthesiology
MODIFICATION TO LR 5200 FILM RECORDER
FDA 510(k)
FDA Class 2
·Radiology
JUGGERKNOT 1.4MM 1 #1 MB 10PK
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code MBI·January 20, 2020
JUGGERKNOT 1.4MM 1 #1 MB 10PK
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code MBI·January 20, 2020
JUGGERKNOT 1.4MM 1 #1 MB 10PK
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code MBI·January 20, 2020
JUGGERKNOT 1.4MM 1 #1 MB 10PK
FDA Adverse Event
Malfunction
·BIOMET ORTHOPEDICS·Product code MBI·August 30, 2017
JUGGERKNOT 1.4MM 1 #1 MB 10PK
FDA Adverse Event
Malfunction
·BIOMET ORTHOPEDICS·Product code MBI·August 30, 2017
PULSE GEN MODEL 102
FDA Adverse Event
Injury
·CYBERONICS, INC.·Product code LYJ·January 11, 2013
BIOGLUE SURGICAL ADHESIVE
FDA Adverse Event
Injury
·CRYOLIFE, INC.·Product code MUQ·December 1, 2010
LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·July 3, 2014
JUGGERKNOT 1.4MM 1 #1 MB 10PK
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code MBI·December 12, 2014
UNK BACTISEAL VENTRICULAR CATHETER
FDA Adverse Event
Injury
·Product code JXG·December 13, 2017
JUGGERKNOT 1.4MM 1 #1 MB 10PK
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBI·February 6, 2018