55 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Disposable Circular Staple, Disposable Hemorrhoidal Stapler, Disposable Linear Stapler and Reloads, Disposable Linear Cutter Stapler and Reloads, Disposable Endoscopic Linear Cutter Stapler and Reloads
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Dornier Thulio Performance Fiber
FDA UDI
INNOVAQUARTZ LLC·00816959021887·
Dornier MedTech
FDA UDI
DORNIER MEDTECH AMERICA, INC.·00810116023448·THULIO LL-R TM 200µM 3M PERF. FIBER 3ST 10X USE
NA
FDA UDI
Synthes GmbH·10886982142177·2.4MM CORTEX SCREW SELF-TAPPING 9MM
Universal CE electrode-patch
FDA UDI
BRAEMAR MANUFACTURING, LLC·B146PE2C0·
ABSORBENT PAPER POINTS
FDA UDI
DiaDent Group International·08806383512732·"An absorbent paper points is an endodontic pap...
LAP-iX
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CG-6108 ACT-IL CONTINUOUS ECG MONITOR AND ARRYTHMIA DETECTOR
FDA 510(k)
FDA Class 2
·Cardiovascular
WALLSTENT ENDOPROSTHESIS WITH UNISTEP PLUS DELIVERY SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code FGE·September 6, 2017
VALIANT STENT GRAFT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·August 1, 2017
ATTAIN ABILITY
FDA Adverse Event
Injury
·MPRI·Product code OJX·June 8, 2017
VAPR HOOK ELECTRODE
FDA Adverse Event
Injury
·DEPUY MITEK·Product code GEI·October 27, 2014
ORTHOPAT PERIOPERATIVE AUTOTRANSFUSION SYSTEM
FDA Adverse Event
Malfunction
·HAEMONETICS CORP.·Product code CAC·August 4, 2011
SYNCHROMED II
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LKK·July 2, 2013
ATTAIN ABILITY
FDA Adverse Event
Injury
·MPRI·Product code OJX·June 8, 2017
GORE VIABAHN® ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code NIP·October 26, 2016
GORE VIABAHN® ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code NIP·October 25, 2016
ATTAIN ABILITY PLUS
FDA Adverse Event
Injury
·MPRI·Product code OJX·June 8, 2017
SELECTSECURE
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code NVN·April 25, 2018
AMPLATZER® TORQVUE® (UNKNOWN)
FDA Adverse Event
Injury
·AGA MEDICAL CORPORATION·Product code DQY·April 23, 2020