从China供应商批发进口Advanced X Ray Table Plxf150 For Fluoroscope — FOB条款

The PLXF150 is a mobile surgical X-ray table designed for C-arm fluoroscopy systems, featuring a bed surface constructed from medical-grade beaverboard that absorbs low-dose X-rays uniformly for clear imaging. The table supports a load capacity of up to 135 kg and includes a gradient bed surface that can be adjusted or removed for convenience during procedures. Its height ranges from 660 mm in the lower position to 910 mm in the upper position, with an ascending and descending range of 250 mm, making it adaptable for various surgical and diagnostic setups.

The table surface measures 1960 mm in length and 586 mm in width, providing ample space for patient positioning while maintaining compatibility with small C-arm systems. The beaverboard material is a standard choice in medical imaging tables due to its X-ray attenuation properties and durability under repeated use. Wheel brake controls allow for easy mobility and stability during operations, a typical feature in mobile surgical tables to ensure safety in hospital environments.

This model is primarily used in hospitals for chest X-rays, surgical procedures, and other diagnostic imaging that requires precise patient alignment under fluoroscopy. Buyers typically include medical facilities upgrading their radiology departments or surgical theaters. The table’s design emphasizes practicality for clinical workflows, with specifications tailored to support C-arm equipment without obstructing the imaging field. Confirm compatibility with specific C-arm models and power requirements before ordering.

Nanjing Perlove Medical Equipment Co., Ltd. is based in Jiangsu Province, China, with its registered address at No.168 Kaiyuan Road, Jiangning Science Park, Nanjing. The company operates from a verified location within a dedicated science park, indicating a focus on medical technology and equipment manufacturing.

The supplier’s profile does not disclose specific certifications, client lists, or production capacity, so buyers should request documentation to confirm compliance with medical device standards. The trust tier classification suggests a baseline level of verification, but direct communication is recommended to assess responsiveness and technical support capabilities.