8 results
·
27ms
·
Sources: EU EUDAMED, US FDA
MEDITRODE KIT
FDA 510(k)
FDA Class 2
·Physical Medicine
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·H65888825541·Dublin Ortho Shoulder Pack
KIMGUARD STERILIZATION WRAP, MODELS KC100, KC200, KC300, KC400, KC500 AND KC600
FDA 510(k)
FDA Class 2
·General Hospital
Powder Free Nitrile Examination Gloves, Blue, Tested for Use with Chemotherapy Drugs
FDA 510(k)
FDA Class 1
·General Hospital
ASR ACETABULAR CUPS 48
FDA Adverse Event
Injury
·DEPUY INTL., LTD. - 8010379·Product code KWA·June 19, 2014
ZENITH AAA ENDOVASCULAR GRAFT BIFURCATED MAIN BODY
FDA Adverse Event
Injury
·COOK INC·Product code MIH·October 22, 2010
MINICAP TRANSFER SET
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDI·December 20, 2012
Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026