8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
RS-3 UNIVERSAL RADIOGRAPHIC WORKING PLACE
FDA 510(k)
FDA Class 2
·Radiology
WORKHORSE II BALLOON CATHETER
FDA Adverse Event
Malfunction
·ANGIODYNAMICS·Product code LIT·January 8, 2008
MININEB
FDA 510(k)
FDA Class 2
·Anesthesiology
PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 14, 2010
3.0MM TI HEADLESS COMPRESSION SCREW 18MM/SHORT THREAD-STER
FDA Adverse Event
Malfunction
·SYNTHES·Product code HWC·January 22, 2013
RECAP CEMENT FMRL HD RESUR 42M
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KXA·July 9, 2014
Azurion 7 M12; Catalog numbers: (1) 722078, (2) 722223, (3) 722233 (OUS ONLY).
FDA Enforcement
Class I
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 26, 2025