1,675 results · 43ms · Sources: EU EUDAMED, US FDA

Light Based Imaging

FDA classification
FDA Class 2 ·Light Based Imaging

Mechanical Compression Device Fecal Incontinence (Non-Manually Operated)

FDA classification
Mechanical Compression Device Fecal Incontinence (Non-Manually Operated)

Enzyme Linked Immunoabsorbent Assay, Rubeola Igg

FDA classification
FDA Class 1 ·Enzyme Linked Immunoabsorbent Assay, Rubeola Igg

Mesh, Surgical, Collagen, Diaphragmatic Hernia

FDA classification
FDA Class 2 ·Mesh, Surgical, Collagen, Diaphragmatic Hernia

Apparatus, Suction, Operating-Room, Wall Vacuum Powered (Export Only)

FDA classification
FDA Not Classified ·Apparatus, Suction, Operating-Room, Wall Vacuum Powered (Export Only)

Mesh, Surgical, Collagen, Plastics, Facial Implants

FDA classification
FDA Class 2 ·Mesh, Surgical, Collagen, Plastics, Facial Implants

Mesh, Surgical, Absorbable, Large Abdominal Wall Defects

FDA classification
FDA Class 2 ·Mesh, Surgical, Absorbable, Large Abdominal Wall Defects

Mesh, Surgical, Collagen, Large Abdominal Wall Defects

FDA classification
FDA Class 2 ·Mesh, Surgical, Collagen, Large Abdominal Wall Defects

Electronic Media, Nausea

FDA classification
FDA Not Classified ·Electronic Media, Nausea

Immunoassay Blood Test For Amyloid Pathology Assessment

FDA classification
FDA Class 2 ·Immunoassay Blood Test For Amyloid Pathology Assessment

Metal Halide Lamp

FDA classification
FDA Not Classified ·Metal Halide Lamp

Multi-Analyte Respiratory Virus Antigen Detection Test

FDA classification
FDA Class 2 ·Multi-Analyte Respiratory Virus Antigen Detection Test

Ecarin Clotting Time

FDA classification
Ecarin Clotting Time

Radiological Image Processing Software For Radiation Therapy

FDA classification
FDA Class 2 ·Radiological Image Processing Software For Radiation Therapy

Extracorporeal System For Carbon Dioxide Removal

FDA classification
FDA Class 2 ·Extracorporeal System For Carbon Dioxide Removal

Device To Detect And Identify Selected Microbial Agents That Cause Acute Febrile Illness

FDA classification
FDA Class 2 ·Device To Detect And Identify Selected Microbial Agents That Cause Acute Febrile Illness

Syringe, Piston, Reprocessed

FDA classification
FDA Class 2 ·Syringe, Piston, Reprocessed

Evoked Photon Image Capture Device

FDA classification
FDA Class 1 ·Evoked Photon Image Capture Device

Device To Detect Or Measure Nucleic Acid From Viruses Associated With Head And Neck Cancers

FDA classification
FDA Class 2 ·Device To Detect Or Measure Nucleic Acid From Viruses Associated With Head And Neck Cancers

Camera, Ophthalmic, General-Use

FDA classification
FDA Class 2 ·Camera, Ophthalmic, General-Use