26 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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U&U Blood Collection Sets
FDA 510(k)
FDA Class 2
·General Hospital
Accufuse Cervical System
FDA UDI
ABSOLUTE ADVANTAGE MEDICAL, LLC·00810016801405·Cervical PEEK 18mmx15mmx8mm 7° Lordosis
Type A Broach Size 15
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215055752·
Omnia Medical TiBrid™-SC
FDA UDI
OMNIA MEDICAL, LLC·00843511104276·TiBrid™-SC ASSEMBLY, 18x15x08mm
OrthoMedFlex
FDA UDI
ORTHOMEDFLEX LLC·M7161111815080·Type A Broach, Size 15
HG OXYGEN CONCENTRATOR, MODELS HG5-W & HG5-WN
FDA 510(k)
FDA Class 2
·Anesthesiology
MODIFICATION TO IBA PROTON THERAPY SYSTEM-PROTEUS 235
FDA 510(k)
FDA Class 2
·Radiology
PRISMALIX
FDA Adverse Event
Malfunction
·MAQUET SAS·Product code FSY·October 17, 2018
Omnia Medical TiBrid™-C
FDA UDI
OMNIA MEDICAL, LLC·00843511101817·18x15x8mm Lordotic cage
ShurFit ACIF 2C
FDA UDI
PRECISION SPINE, INC.·00840019921404·ACIF Trial, 18 x 15 x 8
Omnia Medical TiBrid™-C
FDA UDI
OMNIA MEDICAL, LLC·00843511101572·18x15x8mm Convex cage
IDRT-TS (INTL) 5 PACK 4X5
FDA Adverse Event
Injury
·INTEGRA LIFESCIENCES CORP.·Product code MGR·June 17, 2013
NEPTUNE ROVER
FDA Adverse Event
Malfunction
·STRYKER·Product code FYD·July 25, 2011
ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·CORDIS NEUROVASCULAR, INC.·Product code NJE·September 25, 2008
LIBERTY SELECT CYCLER ASSY(NON-VALUATED)
FDA Adverse Event
Malfunction
·CONCORD MANUFACTURING·Product code FKX·April 19, 2021
LIBERTY SELECT CYCLER ASSY(NON-VALUATED)
FDA Adverse Event
Malfunction
·CONCORD MANUFACTURING·Product code FKX·December 11, 2018
LIBERTY SELECT CYCLER ASSY(NON-VALUATED)
FDA Adverse Event
Malfunction
·CONCORD MANUFACTURING·Product code FKX·November 30, 2018
LIBERTY SELECT CYCLER ASSY(NON-VALUATED)
FDA Adverse Event
Malfunction
·CONCORD MANUFACTURING·Product code FKX·December 3, 2018
LIBERTY SELECT CYCLER ASSY(NON-VALUATED)
FDA Adverse Event
Malfunction
·CONCORD MANUFACTURING·Product code FKX·November 27, 2018
LIBERTY SELECT CYCLER ASSY(NON-VALUATED)
FDA Adverse Event
Malfunction
·CONCORD MANUFACTURING·Product code FKX·September 17, 2020