25 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VENTED VIAL ACCESS DEVICE
FDA 510(k)
FDA Class 2
·General Hospital
N/A
FDA UDI
Smith & Nephew, Inc.·03596010402523·SHOULDER GUIDE 8MM
BETSEY JOHNSON
FDA UDI
FGX INTERNATIONAL INC.·00193033545058·
BETSEY JOHNSON
FDA UDI
FGX INTERNATIONAL INC.·00193033545027·
SIMPLY SPECS
FDA UDI
FGX INTERNATIONAL INC.·00031568633645·
BETSEY JOHNSON
FDA UDI
FGX INTERNATIONAL INC.·00193033545034·
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361013266·PedFuse Remind LES, Quad, 5.0mm x 50mm
SIMPLY SPECS
FDA UDI
FGX INTERNATIONAL INC.·00031568633652·
SIMPLY SPECS
FDA UDI
FGX INTERNATIONAL INC.·00031568633638·
BETSEY JOHNSON
FDA UDI
FGX INTERNATIONAL INC.·00193033545041·
SEEDNET, MODEL FP6T5, FP5T5, FP5T3
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CYPRESS SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
MAMMOVISION CAMERA
FDA Adverse Event
Injury
·FISCHER IMAGING CORP.·Product code IZH·May 14, 1998
KIT IMPLANTABLE SLIM TIP LEAD, 50CM
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code PMP·April 21, 2026
OBM DAB (DIGITAL ACQUISITION BOX)
FDA Adverse Event
Malfunction
·NATUS MEDICAL INCORPORATED·Product code OMC·January 11, 2024
SUPERTORQUE FLUSH CATHETERS
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code DQO·March 20, 2013
TENDRIL SDX
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·March 10, 2011
ONE TOUCH ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·March 14, 2008
TPRLC 133 MP TYPE1 BM HO 13.0
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·May 6, 2022
G7 DUAL MOBILITY LINER 46MM G
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·May 6, 2022