32 results · 30ms · Sources: EU EUDAMED, US FDA

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VENOUS HARDSHELL CARDIOTOMY RESEVOIR, MODEL VHK 4201

FDA 510(k)
FDA Class 2 ·Cardiovascular

STAT KIT Z-1000 EMERGENCY MEDICAL KIT

FDA UDI
HF ACQUISITION CO. LLC·00850065007090·

CAMLOG

FDA UDI
Preat Corporation·00842092103272·CAMLOG® Screw-Line-compatible 5.0/6.0 Guide Pin...

D7-2E Ultrasonic Probe(FDA)

FDA UDI
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.·06944904088389·

IMAGE X-70 PLUS DENTAL X-RAY UNIT

FDA 510(k)
FDA Class 2 ·Dental

EMIT 2000 VALPROIC ACID ASSAY, EMIT 2000 VALPROIC ACID CALIBRATORS, MODEL 4G019UL, 4G109UL

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

POSIFLUSH

FDA Adverse Event
Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 8, 2026

POSIFLUSH

FDA Adverse Event
Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 8, 2026

POSIFLUSH

FDA Adverse Event
Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 8, 2026

POSIFLUSH

FDA Adverse Event
Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 8, 2026

POSIFLUSH

FDA Adverse Event
Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 21, 2026

BD POSIFLUSH

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code NGT·March 20, 2026

BD POSIFLUSH

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code NGT·March 20, 2026

BD POSIFLUSH

FDA Adverse Event
Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 18, 2026

POSIFLUSH

FDA Adverse Event
Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 21, 2026

POSIFLUSH

FDA Adverse Event
Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 25, 2026

TI COLLAR WITH GROOVES

FDA Adverse Event
Malfunction ·SYNTHES BRANDYWINE·Product code MNH·February 28, 2013

VENTRIO-HERNIA PATCH 12.2X10.5X0.3 CM WITH ABSORBAFIX

FDA Adverse Event
Malfunction ·Product code FTL·February 18, 2011

UNKNOWN DEPUY TIBIA

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HSH·February 25, 2008

LANTERN DELIVERY MICROCATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DQY·July 27, 2023