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)