29 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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