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

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ACUITY MAILMAN AND STRAIT-TRAK GUIDEWIRE

FDA 510(k)
FDA Class 2 ·Cardiovascular

TruForm

FDA UDI
Rmo, Inc.·00885797099990·MN 1MOL BD KT U/STD N/LUG 132

POCKET ULTRASONIC OPHTHALMIC PACHYMETER, BIOMETRY TRANSDUCER FOR POCKET

FDA 510(k)
FDA Class 2 ·Radiology

MENISCUS ARROW SHEATH #CN1000A; SMARTSCREW ACL SHEATH #SSA2000A

FDA 510(k)
FDA Class 2 ·Orthopedic

VKMO 78000 3 QUADROX-I HMO 70000+VHK7000

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 25, 2015

VKMO 78000 #QUADROX-I HMO 70000+VHK7000

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 25, 2015

HLM TUBING SET W/SOFTLINE COATING

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DWF·April 6, 2016

LIGACLIP** ENDOSCOPIC CLIP APPLIER

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·May 2, 2013

DURACON UNIVERSAL B/P BEADED

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·September 15, 2014

2800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 26, 2011

EDWARDS ESHEATH INTRODUCER SET

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code NPT·December 6, 2021

EDWARDS TF SHEATH UNKNOWN

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code NPT·October 30, 2021

BD PRECISIONGLIDE¿ NEEDLE

FDA Adverse Event
Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·September 17, 2019

BD¿ NEEDLE 30X1/2 RB

FDA Adverse Event
Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·December 20, 2019