62 results · 24ms · Sources: EU EUDAMED, US FDA

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DIVE AND SHALLOW AND GRAND DIVE

FDA 510(k)
FDA Class 2 ·Anesthesiology

ITI DENTAL IMPLANT SYSTEM

FDA 510(k)
FDA Class 2 ·Dental

ONCOLOGY SALVAGE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

INRATIO

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO INC·Product code GJS·October 26, 2010

INRATIO

FDA Adverse Event
Malfunction ·BIOSITE INCORPORATED·Product code GJS·June 3, 2010

INRATIO

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·July 1, 2011

INRATIO

FDA Adverse Event
Other ·ALERE SAN DIEGO, INC.·Product code GJS·October 26, 2010

OT ULTRALINK METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 23, 2013

INTELLIVUE MULTI MEASUREMENT SERVER X2

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·March 31, 2011

ATTAIN OTW

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWP·July 10, 2008

VANGUARD DA 360 KNEE SYSTEM ARCOM TIBIAL BEARING 71/75 X 14MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JWH·October 7, 2016

RHK SEGMENTAL SHORT YOKE

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JDI·December 7, 2016

INRATIO

FDA Adverse Event
Malfunction ·BIOSITE INCORPORATED·Product code JPA·May 10, 2010

VANGUARD DA 360 KNEE SYSTEM ARCOM TIBIAL BEARING 71/75X14MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JWH·October 7, 2016

VANGUARD DA 360 KNEE SYSTEM ARCOM TIBIAL BEARING 63/67X14MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JWH·October 7, 2016

INRATIO

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·June 12, 2012

VANGUARD DA 360 TIBIAL BEARING ARCM 71/75X16

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JWH·April 28, 2017

INRATIO

FDA Adverse Event
Malfunction ·BIOSITE INCORPORATED·Product code GJS·May 10, 2010

VANGUARD DUAL ARTICULATING (DA) BEARING 71/75 X 16 MM

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JWH·February 6, 2017

INRATIO2 PT MONITORING SYSTEM

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·September 11, 2015