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AUO LCD Cable and Flex RS

5443867
Ultrasonido
LOGIQ P5
GE Sistemas Médicos de México S.A. de C.V
GE HealthCare
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approval number, GE will contact you before your order
can be confirmed for shipment.

Second Opinion Approval Needed

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Approver Name

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OR

Don't know your approval number? Call 800-437-1171
Enter opt 1 for the first three prompts, and have your System ID available.

If you add item(s) to cart and submit your order without
selecting an approver, GE will contact you before your order
can be confirmed for shipment.


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Características

  • Smooth, neat, clear and does not contain any burrs or sharp edges
  • Easy to fix
  • Easily portable
  • ROHS compliant

Descripción del producto

The AUO LCD Cable and Flex RS comes as a part of the Ultrasound imaging systems. It is comprised of a pad, flex board, AUO V2 LVDS Bridge, LCD inverter, AUO LCD harness, display flex board and flex board ferit. The medical Ultrasound images in imaging systems are created by the computer and digital memory from the transmission and reception of mechanical high-frequency waves generated through a probe/transducer. The LCDs are connected to the keyboard by means of the cables. The cable is used as the signal harness. There are Keyboard Board end connector, LCD Panel end connector and Inverter end connector. The wires are tied together by shielding layer and then insulation layer. The GE product is an innovation and technology which fits well into versatile customer needs. The product is securely packaged inside a high quality packing box to avoid physical damage during transit.

©2024 GE HealthCare
1) La información en este material se presenta a modo general, aunque se procura que no existan datos inexactos, pueden existir distintas interpretaciones al respecto; esta información puede ser de aplicación restringida en su país.
2) Los productos mencionados en este material pueden estar sujetos a regulaciones del gobierno y pueden no estar disponibles en todas las localidades. El embarque y la efectiva comercialización únicamente se podrán realizar si el registro del producto ya ha sido otorgado en su país.