Basic Structure and Working Principle of Rigid Endoscopes

Basic Structure and Working Principle of Rigid Endoscopes

09 Feb,2021

Rigid Endoscopes—Shenyang Shenda Endoscopy Co., Ltd. was founded in the 1980s and is one of the earliest domestic manufacturers and developers of medical rigid endoscopes. After more than 30 years of relentless efforts, its range of endoscopes—including the pioneering curved-hose hysteroscope—and associated products have been widely adopted in clinical diagnostics and minimally invasive surgery.

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4K Medical Endoscopic Fluorescence Imaging System

4K Medical Endoscopic Fluorescence Imaging System

25 May,2023

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The impact of the policy on businesses and users

The impact of the policy on businesses and users

11 Dec,2024

Enterprises: Policies provide a solid backing for corporate innovation and development. The special review process for innovative medical devices has significantly shortened the approval cycle for high-end endoscopes, enabling companies to bring their R&D achievements to market more quickly—for instance, Weitong’s intelligent-focus endoscope has been swiftly approved and launched. Meanwhile, the establishment of standardized technical organizations and the dynamic adjustment of product categories have set clear boundaries for corporate R&D, reducing its inherent uncertainty. At the same time, centralized procurement and medical insurance policies are driving enterprises toward transformation. Under the DRG/DIP payment reform, medical institutions increasingly favor cost-effective equipment, prompting companies to shift from simply selling devices to an integrated model that includes “equipment + consumables + services.” Moreover, preferential procurement policies aimed at grassroots-level facilities are guiding enterprises to develop simplified endoscopic products tailored specifically for primary care settings. Additionally, enhanced post-market surveillance requirements are compelling companies to increase their investments in quality testing and adverse event tracing, thereby raising compliance costs.

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The new regulations issued by the National Medical Products Administration regarding high-end medical devices provide strong support for innovation and development in the medical endoscopy industry.

The new regulations issued by the National Medical Products Administration regarding high-end medical devices provide strong support for innovation and development in the medical endoscopy industry.

11 Dec,2024

In addition to the previously effective policies, the new regulations issued by the National Medical Products Administration (NMPA) concerning high-end medical devices provide strong support for innovation and development in the medical endoscopy industry. The key contents, as announced by the NMPA, are as follows: Optimizing Approval and Review Processes: Innovative medical devices—including high-end endoscopes—will undergo a special review process for innovation. Any changes to their registration will also be reviewed under this special procedure. Furthermore, the drafting and revision of technical review guidelines for products such as laparoscopic surgical systems will be expedited, thereby establishing clear standards for the registration and submission of endoscope-related products.

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Future Development Direction

Future Development Direction

11 Dec,2024

Combining industry technology breakthroughs in 2025 with clinical needs-oriented approaches, medical endoscopes will undergo profound evolution in the fields of intelligence and miniaturization, moving toward greater precision, enhanced flexibility, and adaptability to multiple scenarios. At the same time, innovative forms integrating multiple technologies will emerge. The following are specific development directions:

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