8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
NETOH ENDOTRACHEAL TUBE HOLDER
FDA 510(k)
FDA Class 1
·Anesthesiology
AXSOS
FDA UDI
Stryker GmbH·07613327087888·Tag Proximal Medial Tibia
GENTLE SKIN AND (MULTIPLE LABELS) LATEX EXAMINATION GLOVE, POWDER FREE, POLYMER COATED WITH PROTEIN CLAIM
FDA 510(k)
FDA Class 1
·General Hospital
BD PROBETEC NEISSERIA GONORRHOEAE (GC) QX AMPLIFIED DNA ASSAY
FDA 510(k)
FDA Class 2
·Microbiology
FORCETRIAD ENERGY PLATFORM
FDA Adverse Event
Malfunction
·COVIDIEN LP·Product code GEI·April 17, 2014
CLICKX PEDICSCR Ø7 PREASSMBL L45 TAN GRE
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code NKB·February 4, 2013
SHILEY FENESTRATED LOW PRESSURE CUFFED
FDA Adverse Event
Injury
·COVIDIEN/FORMERLY TYCO HEALTHCARE·Product code JOH·December 20, 2010
Captus 4000e Thyroid Uptake System, Model Numbers 5430-30151 and 5430-30152 - Product Usage: is intended to be used by trained nuclear Medicine Technologists or Nuclear Medicine Physicians to perform Thyroid Uptake Procedures.
FDA Enforcement
Class II
·Terminated·Capintec Inc·April 1, 2020