10 results
·
27ms
·
Sources: EU EUDAMED, US FDA
ACCUSCREEN 17-HYDROXYPROGESTERONE
FDA 510(k)
FDA Class 1
·Clinical Chemistry
SeaSpine Spacer System - Hollywood™
FDA UDI
Seaspine Orthopedics Corporation·10889910058328·8mm Hollywood Trial, Lordotic
SeaSpine Spacer System - Hollywood™
FDA UDI
Seaspine Orthopedics Corporation·10889981058326·8mm Hollywood Trial, Lordotic
CORRECTED-V.P.S.
FDA 510(k)
FDA Class 2
·Dental
H.R. JAKOBI SURG. INSTR. #10 34/36
FDA 510(k)
FDA Class 1
·Neurology
PORTEX® BIVONA® AIRE-CUF® NEONATAL AND PEDIATRIC TRACHEOSTOMY TUBE
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code JOH·March 28, 2017
PORTEX®BIVONA® UNCUFFED NEONATAL AND PEDIATRIC TRACHEOSTOSTOMY TUBE
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD INC.,·Product code JOH·June 28, 2016
9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 3, 2013
SPECTRUM INFUSION
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 1, 2014
LIFTING POLE & HANDLE ASSY
FDA Adverse Event
Malfunction
·ARJOHUNTLEIGH·Product code FNL·December 8, 2010