The MyLab™30VETGold, manufactured by Esaote, complies with the Medical Device Directive (MDD) 93\42\EEC. In accordance with this directive, Esaote has classified it as Class IIa devices.
The MyLab™30VETGold ultrasound imaging system was cleared by the Food and Drug Administration (FDA) via 510(k). FDA's review and clearance of MyLab™30Gold Cardiovascular documentation assure that the system meets all FDA requirements.
Technology and features are system/configuration dependent. Specifications subject to change without notice.
Information might refer to products or modalities not yet approved in all countries.
For further details, please contact your Esaote sales representative.
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