35 results
·
21ms
·
Sources: EU EUDAMED, US FDA
FIDIS CELIAC
FDA 510(k)
FDA Class 2
·Immunology
Connecting Tube
FDA UDI
Tianck Medical Co., Ltd.·06971162810452·
LOCATOR R-Tx
FDA UDI
Zest Anchors, LLC·00840481127373·LOCATOR R-Tx Attachment System for BLX, Strauma...
Life Instruments
FDA UDI
Life Instrument Corporation·M930704100200·Surgical Spoon
LOCATOR R-Tx
FDA UDI
Zest Anchors, LLC·00840481128592·LOCATOR R-Tx Abutment, Straumann BLX, 2 mm
CARDINAL HEALTH
FDA UDI
Cardinal Health 200, LLC·10885425620722·DEBRIDEMENT TRAY
PERSONA™
FDA UDI
Zimmer, Inc.·00889024230873·
PERSONA™
FDA UDI
Zimmer, Inc.·00889024230880·
INTUITIVE SURGICAL DA VINCI SURGICAL SYSTEM, MODEL ISI 1000
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
WAKO LIPASE CALIBRATOR
FDA 510(k)
FDA Class 2
·Clinical Chemistry
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