20 results
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44ms
·
Sources: EU EUDAMED, US FDA
Bordetella pertussis dna assay system
FDA registration
MONOCENT INC.·1 product·🇺🇸 United States
ARIES Bordetella Assay; ARIES Bordetella Assay Protocol File Kit
FDA 510(k)
FDA Class 2
·Microbiology
Bordetella Pertussis Dna Assay System
FDA classification
FDA Class 2
·Bordetella Pertussis Dna Assay System
Biomet® Hip System
FDA UDI
Biomet Orthopedics, LLC·00887868308918·
BIOMET HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304256323·
DuraFlex
FDA registration
The Myerson Company Limited·1 product·🇹🇹 Trinidad and Tobago
INSPIRE 6M"
FDA registration
Steril Verona srl·1 product·🇮🇹 Italy
DuraFlex CAD disc
FDA registration
MYERSON LLC·1 product·🇺🇸 United States
INSPIRE 6
FDA registration
SORIN GROUP ITALIA S.R.L·1 product·🇮🇹 Italy
Sklar
FDA UDI
SKLAR CORPORATION·10649111398742·TC KELLY SCISS CVD 6 1/4 INCHES
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587A163626150·16mm H x 36mm W x 26mm L x 15 degrees ALIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587A16362680·16mm H x 36mm W x 26mm L x 8 degrees ALIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587A163626120·16mm H x 36mm W x 26mm L x 12 degrees ALIF
ePlex Respiratory Pathogen (RP) Panel
FDA registration
GENMARK DIAGNOSTICS, INC.·10 products·🇺🇸 United States
Terragene Bionova(R) SCBI (BT220, BT221, BT222, BT223), Terragene Bionova (R) PCD (PCD220-C, PCD220-2, PCD222-C, PCD222-
FDA registration
TUTTNAUER LTD.·1 product·🇮🇱 Israel
ePlex® Respiratory Pathogen (RP) Panel
FDA registration
Hochuen Medical Technology Co.,Ltd.·10 products·🇨🇳 China
DURAFLEX
FDA 510(k)
FDA Class 2
·Dental
CUTERA GENESISPLUS LASER SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Lasers For Temporary Increase Of Clear Nail In Patients With Onychomycosis
FDA classification
FDA Class 2
·Lasers For Temporary Increase Of Clear Nail In Patients With Onychomycosis
Resin, Denture, Relining, Repairing, Rebasing
FDA classification
FDA Class 2
·Resin, Denture, Relining, Repairing, Rebasing