30 results · 25ms · Sources: EU EUDAMED, US FDA

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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