3,175 results
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42ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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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