104 results
·
28ms
·
Sources: EU EUDAMED, US FDA
WELKINS EMT/ICU TEMPERATURE MANAGERMENT SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
UniTip Catheter
FDA UDI
Unisensor AG·07640172973875·
TALOS® HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321217200·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167311217200·
UniTip Catheter
FDA UDI
Unisensor AG·07640172973790·
LG CANNULATED SCREWS
FDA UDI
Smith & Nephew, Inc.·03596010064417·WASHER FOR 8.0MM CANNULATED SCREW
HemoCue® Hb 201+ Analyzer
FDA UDI
Hemocue AB·07311091217202·HemoCue Hb 201+ Analyzer g/L
MULTIVISION METHAFILCON A SOFT (HYDROPILIC) MULTIFOCAL LENS FOR DAILY WEAR
FDA 510(k)
FDA Class 2
·Ophthalmic
JULIET OL
FDA 510(k)
FDA Class 2
·Orthopedic
ARTICULEZE M HEAD 36MM +8.5
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code JDI·April 18, 2018
PINN MAR +4 NEUT 36IDX60OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code LPH·April 18, 2018
HIP REPLACEMENT SYSTEM
FDA Adverse Event
Injury
·DEPUY·Product code JDI·February 1, 2018
ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code LXH·February 10, 2020
MODULAR FEMORAL STEM PLASMA CEMENTLESS SIZE 7.5
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LZO·September 24, 2019
FEMORAL HEAD STERILE PRODUCT DO NOT RESTERILIZE 12/14 TAPER
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·September 24, 2019
MODULAR NECK G1 12/14 NECK TAPER USE WITH +0 HEADS ONLY
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LZO·November 25, 2019
audifon
FDA UDI
audifon GmbH & Co. KG·EADF021771831431217201·RITE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF021137796731217201·BTE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF020715768231217201·BTE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF021142797131217201·BTE-TRT