26 results
·
31ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LPS (LIMB PRESERVATION SYSTEM) LOWER EXTREMITY DOVETAIL INTERCALARY
FDA 510(k)
FDA Class 2
·Orthopedic
Arthrex®
FDA UDI
ARTHREX, INC.·00888867522411·Cannulated Canc Screw,36mm Thd,7.0x85mm
AOS CANNULATED CANCELLOUS SCREW, 36mm THREAD 7.0mm x 85mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665010039·
Myo/Wire II
FDA UDI
A & E MEDICAL CORPORATION·10841291102342·SS Suture, 4 per sleeve
GUIDEWIRE INTRODUCER SAFETY NEEDLE
FDA 510(k)
FDA Class 2
·Cardiovascular
MODIFICATION TO ONYX, FINGER CLIP PULSE OXIMETER, MODEL 9500
FDA 510(k)
FDA Class 2
·Cardiovascular
9616026-2006-00240
FDA Adverse Event
Malfunction
·Product code FII·June 21, 2006
9616026-2006-00244
FDA Adverse Event
Malfunction
·Product code FII·June 22, 2006
FOLYSIL SILICONE CATHETER
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code EZL·January 22, 2025
9616026-2006-00239
FDA Adverse Event
Malfunction
·Product code FII·June 22, 2006
9616026-2006-00222
FDA Adverse Event
Malfunction
·Product code FII·June 21, 2006
PRISMAFLEX SYSTEM
FDA Adverse Event
Malfunction
·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006
PRISMAFLEX SYSTEM
FDA Adverse Event
Malfunction
·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006
PRISMAFLEX SYSTEM
FDA Adverse Event
Malfunction
·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006
9616026-2006-00252
FDA Adverse Event
Other
·Product code FII·June 21, 2006
9616026-2006-00245
FDA Adverse Event
Malfunction
·Product code FII·June 22, 2006
9616026-2006-00253
FDA Adverse Event
Other
·Product code FII·June 21, 2006
PRISMAFLEX SYSTEM
FDA Adverse Event
Malfunction
·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006
FOLYSIL SILICONE CATHETER
FDA Adverse Event
Injury
·COLOPLAST A/S·Product code EZL·October 24, 2024
9616026-2006-00221
FDA Adverse Event
Malfunction
·Product code FII·June 21, 2006