40 results · 21ms · Sources: EU EUDAMED, US FDA

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Model 330 Multifunction Aspirator

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

LEONE SPA

FDA UDI
LEONE SPA·08033707018957·CALIBRA 1ST MOLAR BANDS n.LL 33

VISTA ENDOSCOPE,89 CM, 56CM , SCOUT BLUNT-TIPPED GUIDE- 106 CM, 86 CM, 53 CM, MODELS FG0027, FG0031, FG0029, FG 0028,

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

BTI ENDOSSEOUS DENTAL IMPLANT ANGLED ABUTMENTS

FDA 510(k)
FDA Class 2 ·Dental

INDIGO SYSTEM ASPIRATION CATHETER 5

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·November 21, 2016

INDIGO SYSTEM ASPIRATION CATHETER D

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·February 12, 2019

INDIGO SYSTEM CATD ASPIRATION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·May 29, 2019

INDIGO SYSTEM CATD ASPIRATION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·January 17, 2020

INDIGO SYSTEM ASPIRATION CATHETER D

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·December 7, 2018

INDIGO SYSTEM ASPIRATION CATHETER D

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code QEW·January 29, 2021

INDIGO SYSTEM ASPIRATION CATHETER D

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·December 10, 2020

PENUMBRA SYSTEM JETD REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·June 5, 2019

INDIGO SYSTEM CATD ASPIRATION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·January 25, 2019

INDIGO SYSTEM CATD ASPIRATION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·January 25, 2019

INDIGO SYSTEM CATD ASPIRATION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·July 28, 2020

INDIGO SYSTEM ASPIRATION CATHETER D

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·July 29, 2020

INDIGO SYSTEM CATD ASPIRATION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·September 11, 2020

INDIGO SYSTEM CATD ASPIRATION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DXE·September 24, 2019

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·July 21, 2011

HEARTSTART MRX

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 24, 2013