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Sign in to claim this brandGe Vingmed Ultrasound
US
Last updated May 23, 2026
What Ge Vingmed Ultrasound makes
The company manufactures cardiovascular and general-purpose ultrasound imaging systems, including portable and handheld models for body-surface use. Their product line also includes application software designed for ultrasound imaging, such as EchoPAC, which supports diagnostic analysis and reporting.
These devices are classified as Class II under regulatory frameworks and are listed in the FDA’s 510(k) and UDI registries. The company operates from the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Ge Vingmed Ultrasound manufacture?
Ge Vingmed Ultrasound specializes in ultrasound imaging technology, producing cardiovascular ultrasound imaging systems, general-purpose ultrasound systems, and handheld models designed for body-surface use. Their product line also includes software applications like EchoPAC, which aids in diagnostic analysis and reporting for ultrasound images.
Where is Ge Vingmed Ultrasound based?
The company is headquartered in the United States, where it develops and manufactures its ultrasound imaging devices and related software.
Which regulatory registries list Ge Vingmed Ultrasound’s devices?
Ge Vingmed Ultrasound’s devices are listed in the FDA’s 510(k) premarket notification registry and the FDA’s Unique Device Identifier (UDI) system. These registries track devices that have undergone the required regulatory pathways for market authorization in the US.
How are Ge Vingmed Ultrasound’s devices classified under regulatory frameworks?
Ge Vingmed Ultrasound’s devices fall under Class II classification in regulatory frameworks. This classification applies to devices that generally pose moderate risk and require special controls beyond general controls to ensure safety and effectiveness, such as ultrasound systems used for diagnostic imaging.
AI-generated from registry data and not verified by a human reviewer.
Information
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- US
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Catalogue (59)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Vivid | S70N v202CH | FDA UDI | Class II | Active |
| Vivid | E9 BT11 and BT12 to BT13 XDclear UPG | FDA UDI | Class II | Unknown |
| Vivid | E90 v201 | FDA UDI | Class II | Active |
| Vivid | S60N v205CH | FDA UDI | Class II | Active |
| Vivid | E80 v204 with LCD | FDA UDI | Class II | Active |
| Vivid | S70N v205 | FDA UDI | Class II | Active |
| Vivid | S70N v203 | FDA UDI | Class II | Active |
| Vivid | E v202 to v203 UPG | FDA UDI | Class II | Active |
| System Five/Echopac With Strain Rate Imaging | K991842 | FDA 510(k) | Class II | Active |
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