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

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RED Light Device

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

BI-METRIC HEAD/NECK HIP SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304222953·

Lacrimal Probe

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896103320·French Pattern Lacrimal Probe Bayonet Shaped Si...

ID NOW COVID-19

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCABOROUGH·Product code QJR·November 14, 2021

ID NOW COVID-19

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCABOROUGH·Product code QJR·November 14, 2021

ID NOW COVID-19 ASSAY

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·November 9, 2021

ID NOW COVID-19 ASSAY

FDA Adverse Event
Malfunction ·Product code QJR·November 24, 2021

ID NOW COVID-19 ASSAY

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·November 9, 2021

ID NOW COVID-19 ASSAY

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·November 29, 2021

ID NOW COVID-19 ASSAY

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·November 29, 2021

APEX HCLA ACETABULAR CUP LINERS

FDA 510(k)
FDA Class 2 ·Orthopedic

VANTAGE TITAN 3T

FDA 510(k)
FDA Class 2 ·Radiology

MAXIMO II DR

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·October 10, 2014

HEARTSTART FRX

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 6, 2013

ACUITY

FDA Adverse Event
Injury ·CPI - DEL CARIBE·Product code OJX·July 14, 2011

BI-MET CO-CR HD/NK 13X34X250 R

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code JDI·October 22, 2019

BI-MET CO-CR HD/NK 13X45X200

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code JDI·October 22, 2019

BI-MET CO-CR HD/NK 11X45X250 R

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code JDI·October 22, 2019

REACH 15X250 LT 100% POR FMRL

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·October 22, 2019

MLRY-HD CAL W/HOLE 34X17X220 R

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·October 22, 2019