17 results
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40ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FRAXEL RE:PAIR (FRAXEL III SR) LASER SYSTEM AND ACCESSORIES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
N/A
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994239600·INSTRUMENT 7080915 PLATE COMPRESSOR
N/A
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00763000868161·INSTRUMENT 7080915 PLATE COMPRESSOR
SchureMed
FDA UDI
SCHUERCH CORPORATION·00810014608280·ALLEN, STERIS-AMSCO 2" SOFTCARE
PASTEUR PIPET - STERILE 9, PASTEUR PIPET - STERILE 5 3/4, MODELS 16-PP-9, 16-PP-5.75
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
CDMX
FDA 510(k)
FDA Class 2
·Dental
BD INSYTE AUTOGUARD SHIELDED IV CATHETER
FDA Adverse Event
Other
·BECTON DICKINSON INFUSION THERAPY SYSTEMS, INC.·Product code FOZ·August 9, 2007
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·April 30, 2009
EON MINI
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 23, 2013
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·April 30, 2009
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·August 24, 2009
ACCU-CHEK ® ULTRAFLEX INFUSION SET
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·April 26, 2013
SYNCHRON® LX 20 PRO CLINICAL SYSTEMS
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·May 7, 2011
BALL NOSE GUIDE WIRE 100CM
FDA Adverse Event
Injury
·DEPUY ACE S.A. 'R.L.·Product code LXH·July 22, 2008
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·March 12, 2009
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·October 31, 2008
Cocoon Convective Warming System, Product Code: CWS4000 (110V).
FDA Enforcement
Class II
·Terminated·Care Essentials Pty., Ltd.·February 12, 2020