33 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MODIFICATION TO VERTEX RECONSTRUCTION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·June 13, 2019
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·June 13, 2019
LOCATOR R-Tx
FDA UDI
Zest Anchors, LLC·00840481113635·LOCATOR R-Tx Abutment for 5.0mm Conelog Connect...
Unimed
FDA UDI
Unimed Medical Supplies, Inc.·06936735472116·Disposable NIBP Cuff soft fiber,with double tub...
Unimed
FDA UDI
Unimed Medical Supplies, Inc.·06945664879736·Disposable blood pressure cuff/non-woven fabric...
Unimed
FDA UDI
Unimed Medical Supplies, Inc.·06945664853026·Disposable NIBP Cuff/TPU/Double tube/大Adult/wit...
Unimed
FDA UDI
Unimed Medical Supplies, Inc.·06945664871952·Disposable NIBP Cuff/Textile/Double tube/Large ...
Unimed
FDA UDI
Unimed Medical Supplies, Inc.·06945664854016·Disposable NIBP Cuff/TPU/Double tube/Infant/wit...
Unimed
FDA UDI
Unimed Medical Supplies, Inc.·06936735479320·Disposable NIBP Cuff Double tubes , TPU Cuff, w...
Unimed
FDA UDI
Unimed Medical Supplies, Inc.·06945664853996·Disposable NIBP Cuff/TPU/Double tube/Adult/with...
Unimed
FDA UDI
Unimed Medical Supplies, Inc.·06945664877992·Disposable blood pressure cuff/non-woven/double...
Unimed
FDA UDI
Unimed Medical Supplies, Inc.·06936735472215·Disposable NIBP Cuff soft fiber,with double tub...
Unimed
FDA UDI
Unimed Medical Supplies, Inc.·06945664854009·Disposable NIBP Cuff/TPU/Double tube/Pediatric/...
Unimed
FDA UDI
Unimed Medical Supplies, Inc.·06945664853866·Disposable NIBP Cuff/Textile/Double tube/Adult/...
Unimed
FDA UDI
Unimed Medical Supplies, Inc.·06945664879729·Disposable blood pressure cuff/non-woven fabric...
Unimed
FDA UDI
Unimed Medical Supplies, Inc.·06945664872492·Disposable NIBP Cuff/Textile/Double tube/Thigh/...
9616240-2006-00344
FDA Adverse Event
Malfunction
·Product code KDI·June 14, 2006
9616240-2006-00342
FDA Adverse Event
Malfunction
·Product code KDI·June 14, 2006
9616240-2006-00330
FDA Adverse Event
Malfunction
·Product code FII·June 1, 2006