87 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
COOK PRESSURE MONITORING CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
CliP Partial Prosthesis Titanium
FDA UDI
Heinz Kurz GmbH·EHKM10022541·Ossicular Prosthesis, partial
Procure
FDA UDI
Twin Med, LLC·10840330700501·Small Volume Nebulizer Adult (MVP) Aerosol Mask...
SYRINGE 50ML LL AMBER
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·September 17, 2020
PAR 5 ACETABULAR COMPONENT
FDA 510(k)
FDA Class 2
·Orthopedic
ORTHOMATRIX, INC. CERCLAGE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
IPC® HANDPIECE - XPS® STRAIGHTSHOT® M4
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code ERL·November 15, 2015
MICRODEBRIDER 1898200T IGS M4
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code ERL·May 15, 2014
LINOX SMART SD 60/16
FDA Adverse Event
Injury
·BIOTRONIK SE & CO. KG·Product code NVY·March 13, 2013
ASR ACETABULAR CUPS 50
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 18, 2011
UNKNOWN DEPUY HYLAMER LINER 28X54
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code KWB·February 20, 2008
M/DN®
FDA UDI
Zimmer, Inc.·00889024045729·
M/DN®
FDA UDI
Zimmer, Inc.·00889024045835·
M/DN®
FDA UDI
Zimmer, Inc.·00889024045743·
M/DN®
FDA UDI
Zimmer, Inc.·00889024045583·
M/DN®
FDA UDI
Zimmer, Inc.·00889024045330·
M/DN®
FDA UDI
Zimmer, Inc.·00889024045859·
M/DN®
FDA UDI
Zimmer, Inc.·00889024045699·
M/DN®
FDA UDI
Zimmer, Inc.·00889024045484·
M/DN®
FDA UDI
Zimmer, Inc.·00889024045842·