Introduction
This manual is a reference for the Vivid S70 and Vivid S60 ultrasound systems, covering models Vivid S70 v203 and Vivid S60 v203.
The product complies with regulatory requirements of European Directive 93/42/EEC concerning medical devices.
Certifications and Compliance
GE Medical Systems, Israel Ltd. and GE Medical Systems, China Co. Ltd. are ISO 13485 certified.
The product meets all applicable requirements in relevant EU Directives and European/International standards.
Classified as a Class IIa Medical Device according to 93/42/EEC Medical Device Directive.
Manual:
Download: Vivid S70 / S60 User Manual
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