33 results · 21ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

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