11 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RESO-PAC PERIODONTAL DRESSING
FDA 510(k)
FDA Class 2
·Dental
CT LUCIA
FDA UDI
CARL ZEISS MEDITEC PRODUCTION, LLC·00843045100799·3-piece, monofocal, hydrophobic, acrylic, intra...
ERS RADIAL HEAD REPLACEMENT
FDA 510(k)
FDA Class 2
·Orthopedic
MODIFIED USS FRACTURE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ZILVER 518 BILIARY SELF-EXPANDING STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·September 21, 2017
HEARTSTART HOME
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code NSA·March 14, 2013
SECURE 3 MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·March 14, 2011
RIATA ST ACTIVE FIXATION LEAD
FDA Adverse Event
Death
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 27, 2008
IMPAX CV OUTBOUND (RESULTS MANAGEMENT 2.08)
FDA Adverse Event
Malfunction
·AGFA HEALTHCARE CORP·Product code LLZ·September 17, 2013
ZILVER 518 SELF-EXPANDING STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·October 26, 2012
Belmont Rapid Infuser, a Fluid Management System, Model FMS2000.
FDA Enforcement
Class II
·Terminated·Belmont Instrument Corporation·October 24, 2012