1,652 results · 23ms · Sources: EU EUDAMED, US FDA

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