26 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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COCHLEAR BAHA IMPLANT SYSTEM, COCHLEAR BAHA ATTRACT
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
BIM400 IMPLANT MAGNET
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·December 19, 2017
COCHLEAR BAHA ATTACT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·June 26, 2016
ATTRACT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·October 15, 2015
COCHLEAR BAHA ATTACT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·August 17, 2016
BIM400 IMPLANT MAGNET
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·August 17, 2016
SP MAGNET 3
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·September 13, 2016
COCHLEAR BAHA ATTRACT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·August 14, 2016
BIM400 IMPLANT MAGNET
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·October 8, 2025
COCHLEAR BAHA ATTACT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·August 10, 2016
PIVOX™ Oblique Lateral Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169604933·SPACER 2131240 OLIF25 27MM 6 DEG 10X40
LoFric® Primo™
FDA UDI
Wellspect AB·07392532135477·Single Use Urinary Catheter LoFric Primo Nelato...
LoFric® Primo™
FDA UDI
Wellspect AB·07333387043098·Single Use Urinary Catheter LoFric Primo Nelato...
Excelsior
FDA UDI
MEDLINE INDUSTRIES, INC.·00363807000049·0.9% Sodium Chloride Injection, USP
Vu aPod™ - L
FDA UDI
Seaspine Orthopedics Corporation·10889981046026·LATERAL IMPLANT, ANGLED SPINPLATE™, 12mm X 40mm
CLOSED FUSION PLATE, MTP PLATE, TALUS PLATE, MODEL 824077021, 22; 824677021, 22, 824071001, 824071101, 824671001, 82467
FDA 510(k)
FDA Class 2
·Orthopedic
DISPOSABLE POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVE, BLUE COLOR
FDA 510(k)
FDA Class 1
·General Hospital
DIMENSION® CLINICAL CHEMISTRY SYSTEM
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW·Product code DIP·October 1, 2014
DELTA SHUNT KIT, REGULAR PERFORMANCE LEVEL 1.5
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROSURGERY·Product code JXG·May 23, 2013
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 16, 2011