39 results · 27ms · Sources: EU EUDAMED, US FDA

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SPECTRUM TURBO-JECT PICC SET

FDA 510(k)
FDA Class 2 ·General Hospital

SPECTRUM TURBO-JECT ANTIBIOTIC POWER INJECTABLE PICC

FDA Adverse Event
Injury ·COOK INC·Product code FOZ·April 2, 2019

SPECTRUM TURBO-JECT ANTIBIOTIC POWER INJECTABLE PICC

FDA Adverse Event
Malfunction ·COOK INC·Product code FOZ·March 14, 2018

LJS TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code LJS·May 11, 2018

SPECTRUM TURBO-JECT ANTIBIOTIC POWER INJECTABLE PICC

FDA Adverse Event
Malfunction ·COOK INC·Product code FOZ·February 15, 2018

SPECTRUM TURBO-JECT ANTIBIOTIC POWER INJECTABLE PICC

FDA Adverse Event
Malfunction ·COOK INC·Product code FOZ·February 15, 2018

LJS TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code LJS·May 11, 2018

SPECTRUM TURBO-JECT ANTIBIOTIC POWER INJECTABLE PICC

FDA Adverse Event
Injury ·COOK INC·Product code LJS·June 26, 2017

LJS TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code LJS·May 11, 2018

SPECTRUM TURBO-JECT ANTIBIOTIC POWER INJECTABLE PICC

FDA Adverse Event
Injury ·COOK INC·Product code LJS·July 1, 2017

SPECTRUM TURBO-JECT ANTIBIOTIC POWER INJECTABLE PICC

FDA Adverse Event
Injury ·COOK INC·Product code LJS·February 27, 2020

SPECTRUM TURBO-JECT ANTIBIOTIC POWER INJECTABLE PICC

FDA Adverse Event
Malfunction ·COOK INC·Product code FOZ·February 15, 2018

SPECTRUM TURBO-JECT ANTIBIOTIC POWER INJECTABLE PICC

FDA Adverse Event
Injury ·COOK INC·Product code FOZ·February 13, 2018

SPECTRUM TURBO-JECT ANTIBIOTIC POWER INJECTABLE PICC

FDA Adverse Event
Malfunction ·COOK INC·Product code FOZ·February 15, 2018

Endo Carry-On Procedure Kit

FDA UDI
MEDIVATORS INC.·00677964067983·The ENDO CARRY-ON Procedure Kit contains all of...

RETROGRADE CARDIOPLEGIA CANNULA, MANUAL-INFLATING, WITH MALLEABLE OR GUIDWIRE STYLET

FDA 510(k)
FDA Class 2 ·Cardiovascular

FOWLER ENDOCURETTE, MODEL CUR-XXX

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

OT VERIO TEST STRIPS

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 8, 2013

ECHELON LINEAR CUTTER

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·September 19, 2014

ACCU-CHEK ® COMFORT CURVE TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 24, 2011