33 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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IMMUNOCARD TOXINS A & B, MODEL 712050
FDA 510(k)
FDA Class 1
·Microbiology
ADVANCE®
FDA UDI
Microport Orthopedics Inc.·M684K00410031·
Humeral Cup Stability
FDA UDI
FX SOLUTIONS·03701037309445·HUMERAL CUP STABILITY PE/TA6V Ø40/+3
LOCATOR R-Tx
FDA UDI
Zest Anchors, LLC·00840481127380·LOCATOR R-Tx Attachment System for BLX, Strauma...
Humeral Cup Stability
FDA UDI
FX SOLUTIONS·03701037308042·STABILITY TRIAL CUP Ø40 +3
LATEXX MANUFACTURING SDN. BHD.
FDA registration
LATEXX MANUFACTURING SDN. BHD.·6 products·🇲🇾 Malaysia
LOCATOR R-Tx
FDA UDI
Zest Anchors, LLC·00840481128608·LOCATOR R-Tx Abutment, Straumann BLX, 3 mm
MONTANE TAURUS B-S1.F4 [SZER 120 CM] US
FDA UDI
MEDEN INMED SP Z O O·05903684802425·The MONTANE treatment table is a treatment tabl...
SAFESTING AND SAFESTING HUB
FDA 510(k)
FDA Class 2
·General Hospital
Z-NET
FDA 510(k)
FDA Class 1
·General Hospital
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
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