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

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DJO SURGICAL REVISION FEMORAL HIP SYSTEM, MODEL 428-14/24-140/200; 428-00-050/110;

FDA 510(k)
FDA Class 3 ·Orthopedic

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04047872673174·LEVAMED STABILI-TRI ANK BLU R I

PROFILE-ER

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

ADVIA 120 HEMATOLOGY SYSTEM, CEREBROSPINAL FLUID METHOD

FDA 510(k)
FDA Class 2 ·Hematology

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 10, 2025

NEOCIF INSERTION INSTRUMENT

FDA Adverse Event
Malfunction ·BIOMET SPAIN, S.L.·Product code MQP·November 6, 2018

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 5, 2025

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 13, 2026

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 14, 2026

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 18, 2026

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 19, 2025

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 19, 2025

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 8, 2025

NEOCIF INSERTION INSTRUMENT

FDA Adverse Event
Malfunction ·BIOMET SPAIN, S.L.·Product code MQP·July 20, 2017

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·March 30, 2026

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·March 31, 2026

NC TREK CORONARY DILATATION CATHETER

FDA Adverse Event
Malfunction ·AV-TEMECULA-CT·Product code LOX·May 3, 2013

840 VENTILATOR

FDA Adverse Event
Injury ·COVIDIEN·Product code CBK·August 19, 2014

GOBED II

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FNL·May 3, 2011

PERFUSOR®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 6, 2026