4,373 results
·
35ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
×
Dantec DCN Disposable Concentric Needle Electrodes-25mm, Dantec DCN Disposable Concentric Needle Electrodes-37mm, Dantec DCN Disposable Concentric Needle Electrodes-50mm, Dantec DCN Disposable Concentric Needle Electrodes-75mm
FDA 510(k)
FDA Class 2
·Physical Medicine
MYOVISION 3.0 WIREFREE SYSTEM
FDA 510(k)
FDA Class 2
·Physical Medicine
Hair Boom 69
FDA 510(k)
FDA Class 2
·Physical Medicine
Hair Growth Device
FDA 510(k)
FDA Class 2
·Physical Medicine
BIOPAK MEASUREMENT SYSTEM
FDA 510(k)
FDA Class 2
·Physical Medicine
RE-USABLE BIPOLAR CONCENTRIC NEEDLE(237-XXX-24,237-XXX-24STP, 237-XXX-24TP,237-XXX-24STP
FDA 510(k)
FDA Class 2
·Physical Medicine
Assay, Proliferation, In Vitro, T Lymphocyte
FDA classification
FDA Class 2
·Assay, Proliferation, In Vitro, T Lymphocyte
Gastrointestinal Capsule Endoscopy Analysis Software Device
FDA classification
FDA Class 2
·Gastrointestinal Capsule Endoscopy Analysis Software Device
System, Cystic Fibrosis Transmembrane Conductance Regulator, Gene Mutation Detection
FDA classification
FDA Class 2
·System, Cystic Fibrosis Transmembrane Conductance Regulator, Gene Mutation Detection
Table Mounted Miniaturized Electromechanical Surgical System
FDA classification
FDA Class 2
·Table Mounted Miniaturized Electromechanical Surgical System
System, Cystic Fibrosis Transmembrane Conductance Regulator Gene, Mutations & Variants Panel Sequencing Detection
FDA classification
FDA Class 2
·System, Cystic Fibrosis Transmembrane Conductance Regulator Gene, Mutations & Variants Panel Sequencing Detection
System, Cystic Fibrosis Transmembrane Conductance Regulator Gene, Variant Gene Sequence Detection
FDA classification
FDA Class 2
·System, Cystic Fibrosis Transmembrane Conductance Regulator Gene, Variant Gene Sequence Detection
Upper Arm Electronic Blood Pressure Monitor (U87Y series (models including U80Y, U81Y, U82Y,U83Y,U86Y U80N, U81NH), U86E series (including U82E, U80E, U80EH, U81E, U83E, U85E, U80L, U87E ), U81X series (including U81X, U80X, U82X, U83X, U81D, U82D, U83D, U81RH, U82RH) and U83Z series (including U83Z, U80Z, U81Z, U82Z, U85Z, U86Z and U87Z))
FDA 510(k)
FDA Class 2
·Cardiovascular
Flexor Tuohy-Borst Side-Arm Introducer, Ansel Modification; Flexor Check-Flo Introducer, Ansel Modification; Flexor Check-Flo Introducers, Ansel Modification with High-Flex Dilator and Hydrophilic Coating; Flexor Check-Flo Introducer Balkin Up and Over Contralateral Design; Flexor Up and Over Balkin Contralateral Introducer; Flexor Check-Flo Introducer, Raabe Modification; Flexor Check-Flo Performer Introducer
FDA 510(k)
FDA Class 2
·Cardiovascular
System, Microarray-Based, Genome-Wide, Postnatal Chromosomal Abnormality Detection
FDA classification
FDA Class 2
·System, Microarray-Based, Genome-Wide, Postnatal Chromosomal Abnormality Detection
Kit, Conception-Assist, Home Use
FDA classification
FDA Class 2
·Kit, Conception-Assist, Home Use
Washer, Cleaner, Automated, Endoscope
FDA classification
FDA Class 2
·Washer, Cleaner, Automated, Endoscope
Bed, Air Fluidized
FDA classification
FDA Class 2
·Bed, Air Fluidized
Stimulator, Muscle, Powered, With Limited Output, For Muscle Conditioning
FDA classification
FDA Class 2
·Stimulator, Muscle, Powered, With Limited Output, For Muscle Conditioning
Nonthermal Shortwave Therapy Device Indicated For Over The Counter Use For The Treatment Of Pain
FDA classification
FDA Class 2
·Nonthermal Shortwave Therapy Device Indicated For Over The Counter Use For The Treatment Of Pain