29 results · 22ms · Sources: EU EUDAMED, US FDA

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QUICKLASEDUAL+, QUICKLASE810, QUICKLASE810, QUICKLASE980, QUICKLASE980 MODEL: 3W,5W,3W,5W

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

Bur PM2-70 80K Router 12.8mm sterile

FDA UDI
Bien-Air Surgery SA·J00711004740011·

Bur PM2 80K Router 12.8mm St

FDA UDI
Bien-Air Surgery SA·17630055504293·

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450177952·

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450267356·

SCALP DURA RETRACTOR, MODEL KS00474

FDA 510(k)
FDA Class 2 ·Neurology

Femoral Cutting Block

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215041113·

POWDER FREE VINYL PATIENT EXAMINATION GLOVES, COLORED (YELLOW)

FDA 510(k)
FDA Class 1 ·General Hospital

VIEW NT

FDA 510(k)
FDA Class 2 ·Radiology

ACCU-CHEK ® AVIVA PLUS TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 8, 2013

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 19, 2014

PULSE GEN MODEL 101

FDA Adverse Event
Malfunction ·CYBERONICS, INC.·Product code LYJ·May 13, 2011

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