75 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SOPIX
FDA 510(k)
FDA Class 2
·Dental
SOPIX 2
FDA 510(k)
FDA Class 2
·Dental
Acteon
FDA UDI
DENTAL XRAY COMPANY SRL·08052870660817·
SOPIX INSIDE, SOPIX2 INSIDE
FDA 510(k)
FDA Class 2
·Dental
Acteon
FDA UDI
DENTAL XRAY COMPANY SRL·08052870660916·
ACTEON
FDA UDI
SOPRO·M430S80200051·"The SOPIX series digital X-ray imaging systems...
SCOPIX
FDA registration
SCOPIX·1 product·🇮🇱 Israel
Baichen
FDA UDI
NINGBO BAICHEN MEDICAL DEVICES CO., LTD·06975185620142·
SOLIX
FDA 510(k)
FDA Class 2
·Ophthalmic
SCOPIX VIDEO IMAGER
FDA 510(k)
FDA Class 2
·Radiology
SCOPIX LASER IMAGER
FDA 510(k)
FDA Class 2
·Radiology
Baichen
FDA UDI
NINGBO BAICHEN MEDICAL DEVICES CO., LTD·06975185620111·
Baichen
FDA UDI
NINGBO BAICHEN MEDICAL DEVICES CO., LTD·06975185620128·
Baichen
FDA UDI
NINGBO BAICHEN MEDICAL DEVICES CO., LTD·06975185620104·
SOLIX
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code FTL·November 5, 2012
AUTO SONIX
FDA Adverse Event
Malfunction
·U.S. SURGICAL·Product code LFL·August 21, 2003
AUTO SONIX
FDA Adverse Event
Malfunction
·UNITED STATES SURGICAL·Product code LFL·November 27, 2000
AUTO SONIX
FDA Adverse Event
Malfunction
·UNITED STATES SURGICAL CORP.·Product code GCJ·January 17, 2000
AUTO SONIX
FDA Adverse Event
Other
·UNITED SURGICAL CORP·Product code LFL·March 20, 2001
AUTO SONIX
FDA Adverse Event
Malfunction
·UNITED STATES SURGICAL·Product code LFL·April 28, 2003