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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Otoport/Otocheck Mini Printer (supplied with system)
FDA UDI
OTODYNAMICS LIMITED·05060396170478·
OSTEOMATRIX+
FDA UDI
BIOVENTUS LLC·00816986020129·OSTEOMATRIX+ is a bone graft substitute compris...
OSTEOMATRIX+
FDA UDI
BIOVENTUS LLC·00816986020112·OSTEOMATRIX+ is a bone graft substitute compris...
Otoport/Otocheck Min-Printer Paper Rolls (supplied with system)
FDA UDI
OTODYNAMICS LIMITED·05060396170553·
Otoport/Otocheck Mini-Printer Battery Pack (supplied with system)
FDA UDI
OTODYNAMICS LIMITED·05060396170515·
Otoport/Otocheck Mini-Printer Cable (supplied with system)
FDA UDI
OTODYNAMICS LIMITED·05060396170539·
Otoport/Otocheck Mini Printer
FDA UDI
OTODYNAMICS LIMITED·05060396170485·
Otoport/Otocheck Mini Printer Charger (supplied with system)
FDA UDI
OTODYNAMICS LIMITED·05060396170492·
MICROSCOPE MODEL OM-P
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
QUANTA LITE OMP PLUS ELISA
FDA 510(k)
FDA Class 2
·Immunology
Otoport/Otocheck Mini-Printer Battery Pack
FDA UDI
OTODYNAMICS LIMITED·05060396170522·
Otoport/Otocheck Min-Printer Self-Adhesive Paper Rolls (supplied with system)
FDA UDI
OTODYNAMICS LIMITED·05060396170577·
Otoport/Otocheck Min-Printer Paper Rolls
FDA UDI
OTODYNAMICS LIMITED·05060396170560·
Otoport/Otocheck Mini Printer Charger
FDA UDI
OTODYNAMICS LIMITED·05060396170508·
Otoport/Otocheck Mini-Printer Cable
FDA UDI
OTODYNAMICS LIMITED·05060396170546·
NIHON KOHDEN HEART MONITORS OMP 7101-02
FDA 510(k)
FDA Class 2
·Cardiovascular
ONCENTRA MASTERPLAN
FDA Adverse Event
Malfunction
·NUCLETRON, B.V.·Product code MUJ·December 23, 2011
Otoport/Otocheck Min-Printer Self-Adhesive Paper Rolls
FDA UDI
OTODYNAMICS LIMITED·05060396170584·
ACTIV.A.C. ION PROGRESS REMOTE THERAPY MONITORING SYSTEM
FDA Adverse Event
Injury
·KINETIC CONCEPTS, INC.·Product code OMP·September 8, 2021
V.A.C. DRESSING
FDA Adverse Event
Injury
·KINETIC CONCEPTS, INC.·Product code OMP·June 3, 2021