Disposable Cervical Biopsy Forceps

Intended Use

Mainly used for sampling cervical tissue for pathological examination and screening for diseases such as cervical cancer.

E. H. Spaulding Classification

In 1968, E.H. Spaulding classified medical devices into three categories based on the risk of infection from their use and the required level of disinfection or sterilization between patients: critical items, semi-critical items, and non-critical items. This framework is known as the Spaulding Classification System.

Limitations of Reusable Cervical Biopsy Forceps

• Complex and Cumbersome Design: Their structurally complex and bulky design makes them difficult to manufacture and cumbersome for surgeons to maneuver.

• Risk of Cross-Contamination: As they are not single-use, inadequate disinfection can lead to cross-contamination and iatrogenic infections.

• Risk of Sampling Failure: Due to the distance between the sampling scoop at the end of the shaft and the pivot point of the jaws, the clamping force of the scoop on the targeted cervical tissue is often insufficient, posing a risk of unsuccessful sample collection.

Advantages of Ruitian Single-Use Cervical Biopsy Forceps

• Simple and Ergonomic Design: The simple and rationally designed structure enhances procedural convenience and improves surgical efficiency.

• Superior Performance and Safety: Excellent rigidity and high tensile strength minimize trauma to the local cervical tissue, effectively prevent cross-contamination, and reduce the transmission of various gynecological diseases.

• Precision and Efficacy: Utilizing advanced technology, they enable rapid and accurate tissue sampling with minimal bleeding.