1,652 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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Cytomegalovirus (Cmv) Dna Quantitative Assay
FDA Pre-Market Approval
FDA Class 2
·Abbott RealTime CMV
Cytomegalovirus (Cmv) Dna Quantitative Assay
FDA Pre-Market Approval
FDA Class 2
·Alinity m CMV
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·PERMATINT(R)
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·CUSTOMFLEX CONTACT LENS
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·POLYMACON CONTACT LENSES
Assay, Hybridization And/Or Nucleic Acid Amplification For Detection Of Hepatitis C Rna,Hepatitis C Virus
FDA Pre-Market Approval
FDA Class 2
·RealTime HCV
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·PERMATINT(R)
Sterilizer, Soft-Lens, Thermal, Ac-Powered
FDA Pre-Market Approval
FDA Class 2
·HYDROCURVE PATIENT DISINFECTION UNIT
Assay, Hybridization And/Or Nucleic Acid Amplification For Detection Of Hepatitis C Rna,Hepatitis C Virus
FDA Pre-Market Approval
FDA Class 2
·ABBOTT REAL TIME HBV CALIBRATOR KIT
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·PERMATINT(R)
HMB32 Dialysis Solution
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Sterilizer, Dry Heat
FDA classification
FDA Class 2
·Sterilizer, Dry Heat
Intense Pulsed Light Device For Managing Dry Eye
FDA classification
FDA Class 2
·Intense Pulsed Light Device For Managing Dry Eye
Device, Fluidized Therapy, Dry Heat
FDA classification
FDA Class 2
·Device, Fluidized Therapy, Dry Heat
BioRoot Flow 0.5g, BioRoot Flow 2g
FDA 510(k)
FDA Class 2
·Dental
Biodentine XP 500, Biodentine XP 200
FDA 510(k)
FDA Class 2
·Dental
nCommand Lite System
FDA 510(k)
FDA Class 2
·Radiology
Light Based Device For Dry Age-Related Macular Degeneration
FDA classification
FDA Class 2
·Light Based Device For Dry Age-Related Macular Degeneration
ß-Glucocerebrosidase (Gba) Newborn Screening Test System
FDA classification
FDA Class 2
·ß-Glucocerebrosidase (Gba) Newborn Screening Test System
Intranasal Electrostimulation Device For Dry Eye Symptoms
FDA classification
FDA Class 2
·Intranasal Electrostimulation Device For Dry Eye Symptoms