30 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ACL TIGHTROPE DOUBLE BUNDLE
FDA 510(k)
FDA Class 2
·Orthopedic
NITANIUM ARCHWIRE
FDA UDI
Ortho Organizers, Inc.·00190707057558·.017 x .025 NITANIUM 20° TORQUED ARCHWIRE 38mm...
LIFECARD CF 7 DAY
FDA 510(k)
FDA Class 2
·Cardiovascular
NITRILE EXAMINATION GLOVES, PRE-POWDERED, COLOR BLUE
FDA 510(k)
FDA Class 1
·General Hospital
Widex
FDA UDI
Widex A/S·05706069721713·Widex UNIQUE U-FS BTE (Midnight black S-440 ) T...
Widex
FDA UDI
Widex A/S·05706069722031·Widex D-FS BTE (Midnight black S-440 ) Telecoil...
Widex
FDA UDI
Widex A/S·05706069721225·Widex BEYOND B-F2 (Midnight black S-440 ) Telec...
Widex
FDA UDI
Widex A/S·05706069722451·Widex D-PA BTE (Midnight black S-440 ) RC coil
Widex
FDA UDI
Widex A/S·05706069720945·Widex UNIQUE U-PA BTE (Midnight black S-440 ) R...
AMPLATZER SEPTAL OCCLUDER
FDA Adverse Event
Malfunction
·AGA MEDICAL CORPORATION·Product code MLV·September 8, 2020
AMPLATZER SEPTAL OCCLUDER
FDA Adverse Event
Malfunction
·AGA MEDICAL CORPORATION·Product code MLV·July 29, 2020
AMPLATZER SEPTAL OCCLUDER
FDA Adverse Event
Malfunction
·AGA MEDICAL CORPORATION·Product code MLV·July 29, 2020
WIRELESS BATTERY MODULE G
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·May 1, 2013
THE BELMONT RAPID INFUSER
FDA Adverse Event
Other
·BELMONT INSTRUMENT CORP.·Product code FRN·May 18, 2011
RESTORE RECHARGEABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·August 7, 2008
THROMBUSTER II
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code MMY·March 17, 2014
THROMBUSTER II
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code DXE·October 23, 2012
THROMBUSTER II
FDA Adverse Event
Malfunction
·KANEKA CORP.·Product code DXE·December 21, 2012
THROMBUSTER II
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code DXE·January 16, 2019
EUFLEXXA
FDA Adverse Event
Injury
·BIO-TECHNOLOGY GENERAL (ISRAEL) LTD.·Product code MOZ·February 23, 2015