16 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VIORA V-TOUCH
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Argyle
FDA UDI
Cardinal Health 200, LLC·10192253041804·Arygle Suction Catheter with Directional Contro...
Argyle
FDA UDI
Cardinal Health, Inc.·10884527002580·Suction Catheter with Directional Valve,Straigh...
Tasso+ Convenience Kit
FDA UDI
Tasso Inc.·00850038691042·
UniTip Catheter
FDA UDI
Unisensor AG·07640172971406·
COMPASS F10 SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
SMARTXIDE 50 HS/MS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 28, 2011
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·September 3, 2008
POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025
POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025
POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025
POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025
SMARTXIDE 50 HS
FDA Adverse Event
Malfunction
·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·October 30, 2023
Allegiance Laminated Wood Crutches, item 74151-030, Medium - 43'' - 53''; 1 pair individually shrink wrapped, 10 pairs per case; Distributed by Cardinal Health, McGaw Park, IL 60085-6787 USA, Made in China
FDA Recall
Terminated
·Duro-Med Industries, Inc.·Product code IPR·August 4, 2004