287 results · 42ms · Sources: EU EUDAMED, US FDA

Instrument, Prosthesis Modification For Ossicular Replacement Surgery, Non-Sterile

FDA classification
FDA Class 1 ·Instrument, Prosthesis Modification For Ossicular Replacement Surgery, Non-Sterile

Instrument, Prosthesis Modification For Ossicular Replacement Surgery, Sterile

FDA classification
FDA Class 1 ·Instrument, Prosthesis Modification For Ossicular Replacement Surgery, Sterile

Sunlamp Products (Pre-Standard)

FDA classification
FDA Class 2 ·Sunlamp Products (Pre-Standard)

Laser Products (Pre-Standard)

FDA classification
FDA Not Classified ·Laser Products (Pre-Standard)

Dilator, Vessel, For Percutaneous Catheterization

FDA classification
FDA Class 2 ·Dilator, Vessel, For Percutaneous Catheterization

Antiserum, Fluorescent, Rubeola

FDA classification
FDA Class 1 ·Antiserum, Fluorescent, Rubeola

Computer, Diagnostic, Pre-Programmed, Single-Function

FDA classification
FDA Class 2 ·Computer, Diagnostic, Pre-Programmed, Single-Function

Cement, Bone, Vertebroplasty, Pre-Formed, Modular

FDA classification
FDA Class 2 ·Cement, Bone, Vertebroplasty, Pre-Formed, Modular

Cement, Bone, Pre-Formed, Modular, Polymeric, Vertebroplasty

FDA classification
FDA Class 2 ·Cement, Bone, Pre-Formed, Modular, Polymeric, Vertebroplasty

Whole Blood Pre-Treatment T-Cell Enrichment Reagent

FDA classification
FDA Class 3 ·Whole Blood Pre-Treatment T-Cell Enrichment Reagent

Hydrophilic Re-Coating Solution

FDA classification
FDA Class 2 ·Hydrophilic Re-Coating Solution

Hemodialyzer, Re-Use, High Flux

FDA classification
FDA Class 2 ·Hemodialyzer, Re-Use, High Flux

Hemodialyzer, Re-Use, Low Flux

FDA classification
FDA Class 2 ·Hemodialyzer, Re-Use, Low Flux

Plasma Processing System For Converting Alpha To Pre-Beta High-Density Lipoprotein

FDA classification
Plasma Processing System For Converting Alpha To Pre-Beta High-Density Lipoprotein

Assays To Detect Pre-Existing Antibodies To Adeno-Associated Virus (Aav) Viral Vectors

FDA classification
FDA Class 3 ·Assays To Detect Pre-Existing Antibodies To Adeno-Associated Virus (Aav) Viral Vectors

Spacer, Direct Patient Interface

FDA classification
FDA Class 2 ·Spacer, Direct Patient Interface

Holding Chambers, Direct Patient Interface

FDA classification
FDA Class 2 ·Holding Chambers, Direct Patient Interface

Mitral Valve Repair Devices

FDA classification
FDA Class 3 ·Mitral Valve Repair Devices

Pulmonary Valve Prosthesis Percutaneously Delivered

FDA classification
Pulmonary Valve Prosthesis Percutaneously Delivered

Prosthesis, Mitral Valve, Percutaneously Delivered

FDA classification
FDA Class 3 ·Prosthesis, Mitral Valve, Percutaneously Delivered