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

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MODIFICATION TO ADPER PROMPT

FDA 510(k)
FDA Class 2 ·Dental

HairCheck-DT (THC)

FDA UDI
Quest Diagnostics·00868586000247·HairCheck-DT (THC) is an ELISA test kit used fo...

MAHE PEDIATRIC NASO PHARYNGOSCOPE ITS ASSOCIATED AND ANCILLARY EQUIPMENT AND ENDOSCOPIC ACCESSORIES

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

EECP THERAPY SYSTEM MODEL TS3 WITH PULSE OXIMETRY AND ENHANCED EXTERNAL COUNTERPULSATION EECP MC-2 EXTERNAL COUNTER

FDA 510(k)
FDA Class 2 ·Cardiovascular

EECP THERAPY SYSTEM, MODEL TS3

FDA Adverse Event
Injury ·VASOMEDICAL, INC.·Product code DRN·December 30, 2002

CONFIENT

FDA Adverse Event
Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 8, 2013

TERUMO CDI 500 BLOOD PARAMETER MONITOR

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·March 21, 2011

STERRAD NX STERILIZATION SYSTEM

FDA Adverse Event
Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·May 9, 2008

ST360 SPINAL FIXATION SYSTEM

FDA Adverse Event
Malfunction ·ZIMMER SPINE·Product code MCV·February 27, 2007

UNK HIP FEMORAL STEM CORAIL

FDA Adverse Event
Injury ·DEPUY IRELAND - 9616671·Product code LPH·July 18, 2022

UNKNOWN HIP FEMORAL HEAD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·July 18, 2022

UNKNOWN HIP ACETABULAR LINERS

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·July 18, 2022

UNK HIP ACETABULAR CUP PINNACLE

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·July 18, 2022