29 results
·
29ms
·
Sources: EU EUDAMED, US FDA
MEDI-TRACE DISP. STOPCOCKS/PHYSIO. PRESS
FDA 510(k)
FDA Class 2
·Cardiovascular
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209135578·
ACUMED
FDA UDI
Acumed LLC·10806378051883·Rotational Osteotomy Cutting Guide
VerSys®
FDA UDI
Zimmer, Inc.·00889024144637·
VerSys®
FDA UDI
Zimmer, Inc.·00889024144620·
VerSys®
FDA UDI
Zimmer, Inc.·00889024144613·
VerSys®
FDA UDI
Zimmer, Inc.·00889024144644·
VerSys®
FDA UDI
Zimmer, Inc.·00889024144651·
ZOLL R SERIES BLS DEFIBRILLATOR
FDA 510(k)
FDA Class 3
·Cardiovascular
PARADIGM 1.5ML RESERVOIR, MODEL 326
FDA 510(k)
FDA Class 2
·General Hospital
VerSys®
FDA UDI
Zimmer, Inc.·00889024365193·
VerSys®
FDA UDI
Zimmer, Inc.·00889024365216·
VerSys®
FDA UDI
Zimmer, Inc.·00889024365230·
VerSys®
FDA UDI
Zimmer, Inc.·00889024365209·
VerSys®
FDA UDI
Zimmer, Inc.·00889024365223·
EXCEED ABT E1 FLNG CUP 28X48MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·April 17, 2019
FLEXTEND
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVN·October 23, 2012
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 11, 2014
BATTERY-CAS F/POWER DRIVE F/530.200
FDA Adverse Event
Malfunction
·SYNTHES OBERDORF·Product code MOQ·May 28, 2015
FEMORAL STEM 12/14
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code JDI·November 2, 2021