8 results
·
32ms
·
Sources: EU EUDAMED, US FDA
CORYNEBACTERIA ISOLATION MEDIA
FDA 510(k)
FDA Class 1
·Microbiology
SeaSpine Spacer System (NanoMetalene)- Hollywood, Hollywood VI, Ventura, Pacifica; SeaSpine Spacer System -Hollywood, Hollywood VI, Ventura, Pacifica; SeaSpine Vu e·POD System
FDA 510(k)
FDA Class 2
·Orthopedic
LIISA LEVER INTEGRATED INTERVENTIONAL SYSTEM ADAPTER, MODEL VSL-109
FDA 510(k)
FDA Class 2
·Cardiovascular
DIMENSION RXL MAX WITH HM
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code JJE·June 13, 2014
COLLEAGUE CX VOLUMETRIC INFUSION PUMP SINGLE CHANNEL
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·October 18, 2010
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 13, 2012
M2A MODULAR HEAD COMPONENT 38MM HEAD DIAMETER PLUS 3MM NECK
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·February 10, 2017
IMPACT MODULAR POROUS METAPHYSEAL SEGMENT SIZE 1/ MEDIUM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LPH·February 10, 2017