20 results
·
19ms
·
Sources: EU EUDAMED, US FDA
MYOGRAPH 2000
FDA 510(k)
FDA Class 2
·Anesthesiology
NeoGen
FDA UDI
ENERGIST LIMITED·05060440520242·NeoGen 25mm 3x Nozzle (Black)
iNSitu™ Hip System
FDA UDI
NEXTSTEP ARTHROPEDIX, LLC·00816127020759·Full Hemisphere Reamer Size 58
ENDOSCOPIC ULTRASOUND CENTER EU-Y0008
FDA 510(k)
FDA Class 2
·Radiology
EARLYDETECT MENOPAUSE TEST FOR FSH
FDA 510(k)
FDA Class 1
·Clinical Chemistry
Persona® Revision
FDA UDI
Zimmer, Inc.·00889024630680·
Persona®
FDA UDI
Zimmer, Inc.·00889024559431·
Persona®
FDA UDI
Zimmer, Inc.·00889024559523·
Persona®
FDA UDI
Zimmer, Inc.·00889024630697·
Persona®
FDA UDI
Zimmer, Inc.·00889024559615·
Persona®
FDA UDI
Zimmer, Inc.·00889024630703·
Persona®
FDA UDI
Zimmer, Inc.·00889024559707·
Persona®
FDA UDI
Zimmer, Inc.·00889024630710·
Persona®
FDA UDI
Zimmer, Inc.·00889024558816·
TI LOCKING SCREW
FDA Adverse Event
Injury
·SYNTHES MONUMENT·Product code NKG·June 23, 2017
VNGD CR TIB BRG 10X71/75
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·May 23, 2014
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·November 13, 2012
D-M 1.6MM BEADED CABLE SET VIT
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDCIS CORK·Product code KTT·September 7, 2010
TI LOCKING SCREW
FDA Adverse Event
Injury
·SYNTHES MONUMENT·Product code NKG·June 23, 2017