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

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

ESOPHYX2 HD

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

ESOPHYX Z

FDA Adverse Event
Injury ·ENDOGASTRIC SOLUTIONS, INC.·Product code ODE·June 22, 2017

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526550124·GENUMEDI PT KNEE SUP SILVER L EW III

LACTOSORB* 2.0MM SYSTEM TEMPLATE

FDA UDI
BIOMET MICROFIXATION, INC·00888233011983·

LACTOSORB* 2.0MM SYSTEM TEMPLATE

FDA UDI
BIOMET MICROFIXATION, INC·00841036130763·

SELMAN TISSUE FORCEPS

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896024052·SELMAN TISSUE FORCEPS ROUND CUP TEETH

GE VENUE 40 COMPACT DIAGNOSTIC ULTRASOUND

FDA 510(k)
FDA Class 2 ·Radiology

ZOE FLUID STATUS MONITOR

FDA 510(k)
FDA Class 2 ·Cardiovascular

ONE TOUCH ULTRA MINI TEST STRIPS

FDA Adverse Event
Injury ·Product code CGA·May 15, 2014

OCTRODE

FDA Adverse Event
Injury ·ST JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 28, 2013

EON IMPLANTABLE PULSE GENERATOR

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 25, 2011

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 4, 2014

TECNIS SIMPLICITY

FDA Adverse Event
Injury ·AMO PUERTO RICO MFG. INC.·Product code HQL·February 7, 2023

BD Q-Syte Luer Access Split Septum, 0.16 ml, Sterile, Rx only, Catalog REF #385100, Manufacturer: Becton Dickinson Infusion Therapy Systems Inc. An accessory to an intravascular administration set that permits injection, gravity flow or withdrawal of fluids.

FDA Recall
Terminated ·Becton Dickinson & Company·Product code FPA·February 19, 2015