20 results · 23ms · Sources: EU EUDAMED, US FDA

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BPROSOFT CASP PC SOFTWARE

FDA 510(k)
FDA Class 2 ·Cardiovascular

GALT MEDICAL GUIDEWIRE

FDA 510(k)
FDA Class 2 ·Cardiovascular

JOULE MULTI-PLATFORM SYSTEM

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

ACCESS® HYPERSENSITIVE HTSH

FDA Adverse Event
Malfunction ·BECKMAN COULTER·Product code JLW·May 29, 2013

CAPSUREFIX NOVUS MRI

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO, INC.·Product code NVN·June 16, 2011

FEMORAL CANAL BRUSH

FDA Adverse Event
Injury ·STRYKER INSTRUMENTS PUERTO RICO·Product code FQH·August 20, 2008

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

CARTO® 3 SYSTEM

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·May 21, 2024

CARTO® 3 SYSTEM

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·June 3, 2024

CARTO® 3 SYSTEM

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·April 17, 2024

CARTO® 3 SYSTEM

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·June 3, 2024

CARTO® 3 SYSTEM

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER (ISRAEL) LTD.·Product code DQK·December 22, 2016

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

CARTO® 3 SYSTEM

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·January 10, 2024