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

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I.V. SET-LUER LOCK WITH LATEX FREE INJECTION SITE, MODEL B411

FDA 510(k)
FDA Class 2 ·General Hospital

Implant Prosthetics

FDA UDI
Preat Corporation·00842092104453·Biomet 3i Certain®-compatible 5.0mm Esthetic Ab...

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450179802·

Skan C Mobile C - Arm X - Ray system

FDA UDI
SKANRAY TECHNOLOGIES LIMITED·08904269405519·SKAN-C, is a mobile X-Ray C-Arm fluoroscopic de...

Genio System 2.1

FDA UDI
Nyxoah·05404031018723·The Disposable Patch is a single-use adhesive p...

POLYESTER NONABSORBABLE SURGICAL SUTURES URP

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

DISPOSABLE POWDER FREE VINYL SYNTHETIC EXAM GLOVES, WHITE COLOR

FDA 510(k)
FDA Class 1 ·General Hospital

CONSERVE(R) PLUS HA CUP

FDA Adverse Event
Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWA·November 12, 2013

10 ML BD LUER-LOK¿ SYRINGE WITH 20 G X 1 IN. BD PRECISIONGLIDE¿ NEEDLE

FDA Adverse Event
Injury ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·June 6, 2016

PICC NATE

FDA Adverse Event
Injury ·UTAH MEDICAL PRODUCTS, INC.·Product code LJS·January 12, 2007

PICC NATE

FDA Adverse Event
Injury ·UTAH MEDICAL PRODUCTS, INC.·Product code LJS·January 12, 2007

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 12, 2013

SARNS CENTRIFUGAL PUMP

FDA Adverse Event
TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code KFM·February 18, 2011

EXPRESSEW FLEXIBLE SUTURE PASSER NEEDLE

FDA Adverse Event
Malfunction ·DEPUY MITEK,·Product code HRX·February 25, 2008

CASING FOR 14.4V BATTERY

FDA Adverse Event
Malfunction ·SYNTHES OBERDORF·Product code MOQ·March 18, 2014

IMP,TM 3.7MM MTX,11.5MM

FDA Adverse Event
Malfunction ·ZIMMER DENTAL·Product code DZE·May 5, 2023

PICC-NATE

FDA Adverse Event
Injury ·UTAH MEDICAL PRODUCTS·Product code DQO·April 28, 2004

NEURON MAX 6F 088 LONG SHEATH

FDA Adverse Event
Injury ·PENUMBRA, INC.·Product code DQY·February 18, 2016

Xhibit Telemetry Receiver, Model: 96280

FDA Enforcement
Class II ·Ongoing·Spacelabs Healthcare, Inc.·August 17, 2022

Boston Scientific/Cameron Health SQ-RX Model 1010 subcutaneous pulse generators. The S-ICD System is intended to provide therapy for the treatment of life-threatening ventricular tachyarrhythmias.

FDA Enforcement
Class II ·Terminated·Boston Scientific CRM Corp·March 27, 2013