Import Broncho Fiberscope — Buy in Bulk from Supplier in China

Hangzhou BoWei Medical Equipment Co., Ltd offers a broncho fiberscope designed for endoscopic visualization of the bronchial tree. The device features an improved shade control section to enhance image clarity during procedures. Its ergonomic design and refined working channel positioning allow for precise navigation in clinical settings, reducing patient discomfort.

The fiberscope incorporates high-definition imaging capabilities, which are standard for modern bronchoscopes to ensure diagnostic accuracy. The working channel typically accommodates instruments with a diameter of 2.0 mm or larger, a standard specification for adult bronchoscopes. The device’s distal tip diameter is usually between 4.9 mm and 6.3 mm, depending on the model, with a typical insertion tube length of 600 mm.

This equipment is essential for pulmonology departments in hospitals and clinics, as well as medical research facilities. It supports procedures such as biopsy, foreign body removal, and lavage. Buyers should confirm the exact model specifications, as these are not detailed in the listing. The fiberscope is built for durability, with materials like stainless steel and medical-grade polymers to withstand repeated sterilization cycles.

Hangzhou BoWei Medical Equipment Co., Ltd is based in Hangzhou, Zhejiang Province, China, with an office at Rm1806, No. 1 Building, Zhong Da Plaza. The company is listed as an imported-tier supplier with a harbor trust tier, indicating basic verification. Hangzhou is a major hub for medical device manufacturing, providing access to specialized components and logistics.

The supplier focuses on advanced medical instruments, including endoscopic equipment. Its profile does not specify certifications such as ISO 13485 or CE marking, which are critical for medical devices. The response rate is currently 0%, and no average response time is provided. Buyers should request proof of compliance with international medical device regulations, such as FDA 510(k) clearance or EU MDR certification, before proceeding.