9 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
STABIDENT LOCAL ANESTHESIA SYSTEM
FDA 510(k)
FDA Class 1
·Dental
EDENTA
FDA UDI
EDENTA ETABLISSEMENT·E312K90044610001·Dowel Pin 12 mm
ROCHE ORAL FLUID AMPHETAMINE, ROCHE ORAL FLUID DAT QUAL CAL B, ROCHE ORAL FLUID DAT CONTROL SET B, AND ROCHE ORAL FLUID
FDA 510(k)
FDA Class 2
·Clinical Toxicology
Responsive Arthroscopy Wedge Push-In Suture Anchors
FDA 510(k)
FDA Class 2
·Orthopedic
THAL-QUICK CHEST TUBE SET
FDA Adverse Event
Injury
·COOK INC·Product code GBX·October 16, 2019
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·January 11, 2013
DEFINITION PM CEMENTED HIP #3
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS CORK·Product code JDI·November 23, 2010
NAIL, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code JDS·July 2, 2014
ZILVER PTX 35 DRUG-ELUTING STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code NIU·July 4, 2016