3,175 results · 42ms · Sources: EU EUDAMED, US FDA

Radioimmunoassay, Digoxin (125-I), Rabbit Antibody, Second Antibody Sep.

FDA classification
FDA Class 2 ·Radioimmunoassay, Digoxin (125-I), Rabbit Antibody, Second Antibody Sep.

Set, Dialysis, Single Needle With Uni-Directional Pump, Reprocessed

FDA classification
FDA Class 2 ·Set, Dialysis, Single Needle With Uni-Directional Pump, Reprocessed

Radioimmunoassay, Digoxin (3-H), Rabbit Antibody, Coated Tubes Sep.

FDA classification
FDA Class 2 ·Radioimmunoassay, Digoxin (3-H), Rabbit Antibody, Coated Tubes Sep.

Radioimmunoassay, Digitoxin (125-I), Rabbit Antibody, Solid Phase Sep.

FDA classification
FDA Class 2 ·Radioimmunoassay, Digitoxin (125-I), Rabbit Antibody, Solid Phase Sep.

Radioimmunoassay, Morphine (125-I), Goat Antibody Ammonium Sulfate Sep.

FDA classification
FDA Class 2 ·Radioimmunoassay, Morphine (125-I), Goat Antibody Ammonium Sulfate Sep.

Set, Tubing, Blood, With And Without Anti-Regurgitation Valve

FDA classification
FDA Class 2 ·Set, Tubing, Blood, With And Without Anti-Regurgitation Valve

Radioimmunoassay, Digoxin (125-I), Rabbit Antibody, Solid Phase Sep.

FDA classification
FDA Class 2 ·Radioimmunoassay, Digoxin (125-I), Rabbit Antibody, Solid Phase Sep.

Pediatric/Child Facemask

FDA classification
FDA Class 2 ·Pediatric/Child Facemask

Simple Point-Of-Care Device To Directly Detect Sars-Cov-2 Viral Targets From Clinical Specimens In Near-Patient Settings

FDA classification
FDA Class 2 ·Simple Point-Of-Care Device To Directly Detect Sars-Cov-2 Viral Targets From Clinical Specimens In Near-Patient Settings

Simple Point-Of-Care Device To Detect Sar-Cov-2 Nucleic Acid Targets From Clinical Specimens In Near-Patient Settings

FDA classification
FDA Class 2 ·Simple Point-Of-Care Device To Detect Sar-Cov-2 Nucleic Acid Targets From Clinical Specimens In Near-Patient Settings

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval
FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval
FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval
FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval
FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval
FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535

Test For Detection Of Microorganism(S) Causing Sexually Transmitted Infections Performed By Lay Users

FDA classification
FDA Class 2 ·Test For Detection Of Microorganism(S) Causing Sexually Transmitted Infections Performed By Lay Users

Radioimmunoassay, Digoxin (125-I), Goat Antibody, Anion Exchange, Resin Sep.

FDA classification
FDA Class 2 ·Radioimmunoassay, Digoxin (125-I), Goat Antibody, Anion Exchange, Resin Sep.

Non-Variola Orthopoxvirus Real-Time Pcr Primer And Probe Set

FDA classification
FDA Class 2 ·Non-Variola Orthopoxvirus Real-Time Pcr Primer And Probe Set

Stationary Infrared Thermometer

FDA classification
FDA Class 2 ·Stationary Infrared Thermometer

Device For Home Collection And Transport Of Vaginal Specimens By Lay Users For Use In An Approved Hpv Molecular Assay

FDA classification
FDA Class 2 ·Device For Home Collection And Transport Of Vaginal Specimens By Lay Users For Use In An Approved Hpv Molecular Assay