10 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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V8 Diagnostic Ultrasound System; cV8 Diagnostic Ultrasound System; V7 Diagnostic Ultrasound System; cV7 Diagnostic Ultrasound System; V6 Diagnostic Ultrasound System; cV6 Diagnostic Ultrasound System
FDA 510(k)
FDA Class 2
·Radiology
Cascadia™ Interbody System
FDA UDI
VB Spine LLC·10888857369412·Trial, Size 12x14x6 mm, 0°
2618282-2007-00012
FDA Adverse Event
Malfunction
·Product code KNW·August 17, 2007
Vinyl Examination Gloves (Yellow)
FDA 510(k)
FDA Class 1
·General Hospital
Arthrex Blunt Tip Screws with Fiber Tape
FDA 510(k)
FDA Class 2
·Orthopedic
IMP,TSV,6.0,11.5,MTX,MG
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·September 13, 2023
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·November 9, 2023
PRECISION
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORP·Product code LGW·November 25, 2008
HEARTSTART MRX
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE - ANDOVER·Product code MKJ·July 28, 2011
SECURE II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FNL·July 23, 2013