4,678 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SMOOV O10
FDA 510(k)
FDA Class 2
·Physical Medicine
Echo® Bi-Metric® Hip System
FDA UDI
Biomet Orthopedics, LLC·00887868260476·
ECHO BI-METRIC HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304463394·
Bernafon
FDA UDI
Bernafon AG·05711584086902·ZR3, KIT 312 NFM 90 PB R BE ZERENA 3
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776199876·LLETZ PEDS SPEC L ET
OsteoMed
FDA UDI
OSTEOMED LLC·00845694009614·2.0mm x 16mm Cannulated Lag Screw
OsteoMed
FDA UDI
OSTEOMED LLC·00845694070225·Cannulated 2.0 x 16mm Lag Screw Sterile Qty 5
SUPER-FINE PEN NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
PRECICONTROL CLINCHEM MULTI 1 AND 2
FDA 510(k)
FDA Class 1
·Clinical Chemistry
UNKNOWN DEPUY INSERT
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JWH·October 6, 2008
DUROM HIP GENERIC
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·June 20, 2013
RF3000 RADIOFREQUENCY GENERATOR
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code GEI·August 4, 2011
COCHLEAR BAHA CONNECT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·September 18, 2016
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code OYC·November 11, 2016
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code OYC·September 13, 2016
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·May 2, 2016
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code OYC·September 16, 2016
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·August 15, 2016
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 1, 2016
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·October 13, 2016