20 results
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33ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ALN Straight RS
FDA UDI
A.L.N.·03760017680103·The device is a Straight Extraction Kit of ALN ...
ALN Optional Vena Cava Filter - Brachial Approach
FDA UDI
A.L.N.·03760017680028·The device is an Optional Vena Cava Filter - Br...
ALN Optional Vena Cava Filter - Jugular Approach with Hook
FDA UDI
A.L.N.·03760017680059·The device is an Optional Vena Cava Filter - Ju...
ALN 2in1
FDA UDI
A.L.N.·03760017680127·The device is a 2in1 Extraction Kit of ALN Vena...
ALN Optional Vena Cava Filter - Jugular Approach
FDA UDI
A.L.N.·03760017680011·The device is an Optional Vena Cava Filter - Ju...
ALN Optional Vena Cava Filter - Brachial Approach with Hook
FDA UDI
A.L.N.·03760017680066·The device is an Optional Vena Cava Filter - Br...
ALN Optional Vena Cava Filter - Femoral Approach with Hook
FDA UDI
A.L.N.·03760017680042·The device is an Optional Vena Cava Filter - Fe...
ALN Pre-Curved RS
FDA UDI
A.L.N.·03760017680110·The device is a Pre-curved Extraction Kit of AL...
ALN Optional Vena Cava Filter - Femoral Approach
FDA UDI
A.L.N.·03760017680004·The device is an Optional Vena Cava Filter - Fe...
A.L.N.
FDA Adverse Event
Death
·A.L.N. IMPLANTS CHIRURGICAUX·Product code DTK·February 7, 2019
ALN OPTIONAL VENA CAVA FILTER
FDA Adverse Event
Injury
·A.L.N.·Product code DTK·May 13, 2019
ALI ULTRAPACS DIAGNOSTIC REPORTING CLIENT SOFTWARE
FDA Adverse Event
Malfunction
·A.L.I. TECHNOLOGIES, INC.·Product code LNX·February 19, 1999
Horizon AF Plus System (Integrated A.L. One AF Plus OXYGENATOR and Horizon CVR) (US5300); A.L. One AF Plus OXYGENATOR (US5204); Horizon CVR (US5073)
FDA 510(k)
FDA Class 2
·Cardiovascular
ADVANCED BIONICS U.S. PAT. 366 HIRES 9011
FDA Adverse Event
Injury
·CANNON TECHNOLOGIES INC·Product code MCM·April 23, 2010
CEILING MOUNTED EXAM LIGHT
FDA Adverse Event
A.L.M. SURGICAL·Product code FSY·March 22, 1995
ALI WEB GX VERSION 3.0
FDA Adverse Event
Injury
·A.L.I. TECHNOLOGIES, INC.·Product code LNX·January 9, 2003
ALI ULTRAPACS GX V3.2 MEDICAL IMAGE VIEWER
FDA Adverse Event
Malfunction
·A.L.I. TECHNOLOGIES, INC.·Product code LNX·January 9, 2003
ALI ULTRAPACS GX V3.2 MEDICAL IMAGE VIEWER
FDA Adverse Event
Malfunction
·A.L.I. TECHNOLOGIES, INC.·Product code LNX·January 9, 2003
ALI ULTRAPACS DIAGNOSTIC REPORTING CLIENT SOFTWARE
FDA Adverse Event
Malfunction
·A.L.I. TECHNOLOGIES, INC.·Product code LNX·January 9, 2003
TECNIS IOL
FDA Adverse Event
Injury
·AMO MANUFACTURING NETHERLANDS·Product code MFK·October 1, 2021