28 results
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37ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FRONTIER DEVICES FUSIO SCREW FUZE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PILLING
FDA UDI
TELEFLEX INCORPORATED·24026704508291·OPERATING SCISSORS STRAIGHT SHARP/SHARP 5 1/2"
Urethral Warming Catheter Kit
FDA UDI
VARIAN MEDICAL SYSTEMS, INC.·00810563020977·Urethral Warming catheter for use in tissue war...
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167311411060·
TALOS® HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321411060·
SCHWERT
FDA UDI
A. Schweickhardt GmbH & Co. KG·E8961411060·Spiculum Raspatory/round Periostelevator
curved...
3M™ Unitek™
FDA UDI
3M UNITEK CORPORATION·00652221036773·Unitek(TM) Bicuspid Band General Purpose Narrow...
POWDERED, NATURAL COLOR, LATEX EXAMINATION GLOVE MODEL: MEP1
FDA 510(k)
FDA Class 1
·General Hospital
REVISION KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
VACUTRON
FDA UDI
Allied Medical, LLC·00026072006337·HIGH VACUUM SUCTION REGULATOR
DIGITAL RADIOGRAPHY CXDI
FDA Adverse Event
Malfunction
·CANON, INC.·Product code MQB·December 22, 2019
VACUTRON
FDA UDI
Allied Medical, LLC·00026072006368·HIGH VACUUM SUCTION REGULATOR
VACUTRON
FDA UDI
Allied Medical, LLC·00026072006382·HIGH VACUUM SUCTION REGULATOR
VACUTRON
FDA UDI
Allied Medical, LLC·00026072006375·HIGH VACUUM SUCTION REGULATOR
VACUTRON
FDA UDI
Allied Medical, LLC·00026072006351·HIGH VACUUM SUCTION REGULATOR
VACUTRON
FDA UDI
Allied Medical, LLC·00026072006344·HIGH VACUUM SUCTION REGULATOR
DIGITAL RADIOGRAPHY CXDI
FDA Adverse Event
Malfunction
·CANON, INC.·Product code MQB·December 22, 2019
DIGITAL RADIOGRAPHY CXDI
FDA Adverse Event
Malfunction
·CANON, INC.·Product code MQB·December 22, 2019
BELLAVISTA
FDA Adverse Event
Injury
·IMTMEDICAL AG·Product code CBK·September 28, 2021
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·June 3, 2013