4,637 results
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47ms
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Sources: EU EUDAMED, US FDA
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Classification: FDA Class 2
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Neonatal Icu Continuous Non-Invasive Blood Pressure Monitor (Includes Alarms)
FDA classification
FDA Class 2
·Neonatal Icu Continuous Non-Invasive Blood Pressure Monitor (Includes Alarms)
Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate
FDA classification
FDA Class 2
·Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate
Integrated Continuous Glucose Monitor For Non-Intensive Glucose Monitoring, Over-The-Counter
FDA classification
FDA Class 2
·Integrated Continuous Glucose Monitor For Non-Intensive Glucose Monitoring, Over-The-Counter
Shoulder Spacer For Massive Irreparable Rotator Cuff Tear, Resorbable, Inflatable, Non-Fixed
FDA classification
FDA Class 2
·Shoulder Spacer For Massive Irreparable Rotator Cuff Tear, Resorbable, Inflatable, Non-Fixed
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
FDA classification
FDA Class 2
·Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Integrated Continuous Glucose Monitor For Non-Intensive Glucose Management, Over-The-Counter
FDA classification
FDA Class 2
·Integrated Continuous Glucose Monitor For Non-Intensive Glucose Management, Over-The-Counter
Substance, Blood Grouping Of Non-Human Origin For In Vitro Diagnostic Use
FDA classification
FDA Class 2
·Substance, Blood Grouping Of Non-Human Origin For In Vitro Diagnostic Use
Manual Instruments Designed For Use With Non-Fusion Spinous Process Spacer Devices
FDA classification
FDA Class 2
·Manual Instruments Designed For Use With Non-Fusion Spinous Process Spacer Devices
Mesh, Surgical, Non-Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator
FDA classification
FDA Class 2
·Mesh, Surgical, Non-Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator
Non-Implanted Nerve Stimulator For Pain Associated With Irritable Bowel Syndrome (Ibs)
FDA classification
FDA Class 2
·Non-Implanted Nerve Stimulator For Pain Associated With Irritable Bowel Syndrome (Ibs)
Monitor, Oxygen, Cutaneous, For Uses Other Than For Infant Not Under Gas Anesthesia
FDA classification
FDA Class 2
·Monitor, Oxygen, Cutaneous, For Uses Other Than For Infant Not Under Gas Anesthesia
Mesh, Surgical, Non-Synthetic, Urogynecologic, For Apical Vaginal And Uterine Prolapse, Transabdominally Placed
FDA classification
FDA Class 2
·Mesh, Surgical, Non-Synthetic, Urogynecologic, For Apical Vaginal And Uterine Prolapse, Transabdominally Placed
System, Nucleic Acid Amplification Test, Dna, Carbapenem Non-Susceptible Gram Negative Organism, Colony
FDA classification
FDA Class 2
·System, Nucleic Acid Amplification Test, Dna, Carbapenem Non-Susceptible Gram Negative Organism, Colony
Nucleic Acid Detection System For Non-Viral Microorganism(S) Causing Sexually Transmitted Infections
FDA classification
FDA Class 2
·Nucleic Acid Detection System For Non-Viral Microorganism(S) Causing Sexually Transmitted Infections
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous Cemented, Osteophilic Finish
FDA classification
FDA Class 2
·Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous Cemented, Osteophilic Finish
Integrated Continuous Glucose Monitoring System, Factory Calibrated, Not For Use With Automated Insulin Delivery Systems
FDA classification
FDA Class 2
·Integrated Continuous Glucose Monitoring System, Factory Calibrated, Not For Use With Automated Insulin Delivery Systems
System For Detection Of Nucleic Acid From Non-Viral Microorganism(S) Causing Stis Using Specimens Collected At Home
FDA classification
FDA Class 2
·System For Detection Of Nucleic Acid From Non-Viral Microorganism(S) Causing Stis Using Specimens Collected At Home