BESDATA Achieves FDA 510(k) Clearance for Four Single-Use Flexible Ureteroscope

BESDATA is proud to announce that our Single-use Flexible Ureteroscope models—UR-D1, UR-D2, UR-F1, and UR-F2—have successfully received FDA 510(k) certification, marking a significant milestone in our mission to provide safe and reliable medical solutions to healthcare professionals worldwide. This certification reaffirms the safety and effectiveness of BESDATA's ureteroscopes, now cleared for use in the U.S. market.

As a global leader in endoscopic technology, BESDATA remains committed to developing innovative, cost-effective solutions that enhance patient care while adhering to stringent regulatory standards. Our single-use flexible ureteroscopes deliver exceptional visualization and ease of use, addressing the growing need for advanced, disposable devices in urology.

We invite attendees of MEDICA 2024 to visit our booth, where we will be showcasing these newly certified models alongside our full range of cutting-edge endoscopic products. Don't miss the chance to explore how BESDATA is pushing the boundaries of medical technology and improving healthcare outcomes worldwide.

Key Highlights:

• FDA 510(k) clearance for four single-use flexible ureteroscope models (UR-D1, UR-D2, UR-F1, UR-F2)
• Enhanced visualization and disposable design for better infection control
• Commitment to delivering affordable, high-quality medical solutions globally

We look forward to connecting with healthcare professionals and partners at MEDICA 2024. Be sure to stop by our booth for product demonstrations and in-depth discussions on how our ureteroscope solutions can support your clinical needs.