10 results
·
25ms
·
Sources: EU EUDAMED, US FDA
DIGOXIN-EIA-XT
FDA 510(k)
FDA Class 2
·Clinical Toxicology
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756731294·CATARACT PACK CSM
TROJAN FOR WOMEN
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
PATIENT EXAM GLOVE (MFG. DALIAN LATEX & JIN ZHOU)
FDA 510(k)
FDA Class 1
·General Hospital
ALTRX NEUT 36IDX52OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·June 26, 2014
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 4, 2013
PROMUS ELEMENT EVEROLIMUS-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·November 11, 2010
DeRoyal CATARACT PACK CSM, REF 89-6863
FDA Recall
Open, Classified
·DeRoyal Industries Inc·Product code LRO·November 3, 2022
DeRoyal CATARACT PACK CSM, REF 89-6863
FDA Enforcement
Class II
·Ongoing·DeRoyal Industries Inc·December 21, 2022
Daig Livewire Steerable, Product Number 401915; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026