23 results · 21ms · 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.

EBV-EBNA IGG ELISA KIT, MODEL EBG-100

FDA 510(k)
FDA Class 1 ·Microbiology

Cook

FDA UDI
COOK INCORPORATED·00827002158733·Urodynamics Catheter

3M™ Unitek™

FDA UDI
3M UNITEK CORPORATION·00652221231383·Unitek Miniature Twin MBT UL Bi -7T/0A DHk 022 MMT

Single Use Biliary Stent V

FDA UDI
OLYMPUS MEDICAL SYSTEMS CORP.·04953170186059·Single Use Biliary Stent V

M6-C

FDA UDI
Spinal Kinetics, Inc.·00812388031206·Fin Cutter, 6LL (6mm H x 17mm W x 16mm D), G7

Cook

FDA UDI
COOK INCORPORATED·00827002169876·Urodynamic Balloon Catheter Triple Lumen With C...

Cook

FDA UDI
COOK INCORPORATED·00827002161696·Urodynamics Catheter

Cook

FDA UDI
COOK INCORPORATED·00827002157392·Urodynamics Catheter

Cook

FDA UDI
COOK INCORPORATED·00827002154353·Urodynamics Catheter

Cook

FDA UDI
COOK INCORPORATED·00827002171749·Urodynamics Catheter

Cook

FDA UDI
COOK INCORPORATED·00827002155404·Urodynamic Balloon Catheter Triple Lumen

PVS 1400 GUIDE WITE WITH HYDROPHILIC COATING

FDA 510(k)
FDA Class 2 ·Cardiovascular

LEICA COLPOSCOPE

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·December 30, 2015

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·May 1, 2014

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDIC, INC.·Product code KWP·August 1, 2011

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·May 15, 2013

DAILY ACTIVITY ASSIST DEVICES

FDA Adverse Event
UNKNOWN·Product code IKX·July 6, 2012

HOLLOW FIER OXYGENATOR W/3000 ML

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTZ·March 18, 2013

HEARTMATE II LVAS

FDA Adverse Event
Injury ·THORATEC CORPORATION·Product code DSQ·March 16, 2011