46 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Gastric Irrigation And Aspiration Kit
FDA classification
FDA Class 2
·Gastric Irrigation And Aspiration Kit
Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
FDA classification
FDA Class 2
·Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
Prosthesis, Wrist, 2 Part Metal-Plastic Articulation, Semi-Constrained
FDA classification
FDA Class 2
·Prosthesis, Wrist, 2 Part Metal-Plastic Articulation, Semi-Constrained
Prosthesis, Wrist, 3 Part Metal-Plastic-Metal Articulation, Semi-Constrained
FDA classification
FDA Class 2
·Prosthesis, Wrist, 3 Part Metal-Plastic-Metal Articulation, Semi-Constrained
Device To Detect And Measure Procalcitonin (Pct) In Human Clinical Specimens
FDA classification
FDA Class 2
·Device To Detect And Measure Procalcitonin (Pct) In Human Clinical Specimens
Light, Lymphedema Reduction, Low Energy
FDA classification
FDA Class 2
·Light, Lymphedema Reduction, Low Energy
Antigen, Inflammatory Response Marker, Sepsis
FDA classification
FDA Class 2
·Antigen, Inflammatory Response Marker, Sepsis
Endoscopic Storage Cover
FDA classification
FDA Class 2
·Endoscopic Storage Cover
Tubing, Long Term Support Greater Than 6 Hours
FDA classification
FDA Class 2
·Tubing, Long Term Support Greater Than 6 Hours
Ankle Fusion Cage
FDA classification
FDA Class 2
·Ankle Fusion Cage
Prosthesis, Knee, Femorotibial, Unicompartmental/Unicondylar, Uncemented, Porous-Coated, Metal/Polymer
FDA classification
FDA Class 2
·Prosthesis, Knee, Femorotibial, Unicompartmental/Unicondylar, Uncemented, Porous-Coated, Metal/Polymer
Sacroiliac Joint Guidewire Placement Device
FDA classification
FDA Class 2
·Sacroiliac Joint Guidewire Placement Device
Suntan Bed
FDA classification
FDA Class 2
·Suntan Bed
Hematopoietic Cell Enrichment Kit
FDA classification
FDA Class 2
·Hematopoietic Cell Enrichment Kit
Assay To Measure Pct To Aid In The Risk Assessment Of Critically Ill Patients On Their First Day Of Icu Admission
FDA classification
FDA Class 2
·Assay To Measure Pct To Aid In The Risk Assessment Of Critically Ill Patients On Their First Day Of Icu Admission
Intravenous Catheter Force-Activated Separation Device.
FDA classification
FDA Class 2
·Intravenous Catheter Force-Activated Separation Device.
Radiology Software For Referral Of Findings Related To Fibrotic Lung Disease.
FDA classification
FDA Class 2
·Radiology Software For Referral Of Findings Related To Fibrotic Lung Disease.
Blood Pump For Ecmo, Long-Term (> 6 Hours) Use
FDA classification
FDA Class 2
·Blood Pump For Ecmo, Long-Term (> 6 Hours) Use
Cardiovascular Machine Learning-Based Notification Software
FDA classification
FDA Class 2
·Cardiovascular Machine Learning-Based Notification Software
21-Hydroxylase Antibody (21-Ohab)
FDA classification
FDA Class 2
·21-Hydroxylase Antibody (21-Ohab)