29 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.

PEDIATRIC CUFFED AND UNCUFFED ET TUBES; STANDARD CUFFED AND UNCUFFED ET TUBES

FDA 510(k)
FDA Class 2 ·Anesthesiology

Citrine Triple Quad™ MS/MS

FDA UDI
AB SCIEX (MANUFACTURING)·00842365100533·The Citrine system is a liquid chromatography-t...

LOCATOR F-Tx

FDA UDI
Zest Anchors, LLC·00840481121067·LOCATOR F-Tx Abutment For Wide Platform (WP) In...

LOCATOR R-Tx

FDA UDI
Zest Anchors, LLC·00840481113871·LOCATOR R-Tx Abutment for Wide Platform (WP) In...

Neo-Tee T-Piece Resuscitator

FDA UDI
MERCURY ENTERPRISES, INC.·10641043508039·

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450266212·

LOCATOR R-Tx

FDA UDI
Zest Anchors, LLC·00840481128981·LOCATOR R-Tx Abutment, WP Conical Connection, 3...

CAPSTONE SPINAL SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·May 1, 2018

CT/MR Henschke Right Colpostat w/ bracket, Varian

FDA UDI
MICK RADIO NUCLEAR INSTRUMENT, INC·00817330020857·

CT/MR Henschke Left Colpostat w/ bracket, Varian

FDA UDI
MICK RADIO NUCLEAR INSTRUMENT, INC·00817330020864·

POWDER-FREE LATEX EXAMINATION GLOVES-BLUE COLOR

FDA 510(k)
FDA Class 1 ·General Hospital

CEFAR MEDICAL AB CEFAR PRIMO

FDA 510(k)
FDA Class 2 ·Neurology

CAPSTONE SPINAL SYSTEM

FDA Adverse Event
Injury ·MSD DEGGENDORF MFG·Product code MAX·April 19, 2018

LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC·Product code LDD·April 10, 2013

TENDRIL SDX

FDA Adverse Event
Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·May 27, 2008

SYMPHONY

FDA Adverse Event
Injury ·SORIN CRM·Product code NVZ·April 1, 2011

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDIC, INC.·Product code NQP·September 7, 2012

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code NQP·July 6, 2012

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code NQP·July 6, 2012

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDIC, INC.·Product code NQP·July 6, 2012