BD LA101-RLL - Insufflation Tubing, Rotating Luer Lock, 0.1 Micron Filter, 10 ft, Sterile 20/BX (Temp Sensitive; Non-Returnable)
The BD LA101-RLL Insufflation Tubing is a single-use surgical tubing set designed to support controlled gas delivery during compatible laparoscopic and minimally invasive surgical procedures. The system features a rotating Luer lock connection, an integrated 0.1-micron hydrophobic filter, and a 10-foot tubing length to support flexible equipment positioning within the operating room.
The rotating Luer lock connection supports secure attachment while allowing rotational movement that can help reduce unwanted tubing twist during setup and use. The 10-foot length provides flexibility when positioning compatible insufflation equipment in relation to the operating table and procedural field.
The integrated bidirectional 0.1-micron hydrophobic filter is designed to help reduce the chance of contamination within the insufflation pathway. The tubing is supplied sterile and is not made with natural rubber latex, supporting use within established surgical and infection-prevention protocols.
The BD LA101-RLL is packaged 20 units per box, providing a practical supply configuration for hospitals, operating rooms, ambulatory surgery centers, and other facilities that routinely perform laparoscopic procedures.
Key Benefits
- 0.1-micron hydrophobic filter supports filtration within the insufflation gas pathway.
- Bidirectional filter design helps reduce the chance of contamination during appropriate use.
- Rotating Luer lock connection supports secure attachment and flexible tubing positioning.
- Ten-foot tubing length provides flexibility for operating room equipment placement.
- Single-use configuration supports efficient procedural turnover and eliminates the need for tubing reprocessing.
- Sterile presentation supports established aseptic surgical workflows.
- Not made with natural rubber latex for facilities managing latex-related product requirements.
- Designed for integration into compatible laparoscopic and minimally invasive surgical procedures.
- Twenty units per box support inventory planning for high-volume surgical departments.
Compatibility and Applications
The BD LA101-RLL Insufflation Tubing is intended for use with compatible insufflation equipment and laparoscopic systems that accept the applicable Luer lock connection. Compatibility should be confirmed with the insufflator, surgical access device, and other connected equipment before use.
Typical applications include laparoscopic and other minimally invasive procedures requiring controlled delivery of insufflation gas to establish or maintain an operative working space.
The product may be used in general surgery, gynecologic surgery, urologic procedures, bariatric surgery, and other laparoscopic specialties when the tubing configuration is appropriate for the equipment and procedure.
Typical healthcare environments include hospital operating rooms, ambulatory surgery centers, specialty surgical facilities, and other controlled procedural settings. Healthcare professionals should not assume universal compatibility with every insufflator or access system and should confirm connector, flow, and equipment requirements before use.
Usage Guidelines
Before use, confirm the BD LA101-RLL catalog number, 0.1-micron filter configuration, 10-foot tubing length, rotating Luer lock connection, sterile package integrity, and compatibility with the intended insufflation equipment.
- Inspect the sterile packaging, tubing, filter, and connectors before use.
- Do not use the product if the sterile barrier is damaged, opened, wet, punctured, or otherwise compromised.
- Connect the tubing only to compatible insufflation equipment and surgical access components.
- Secure the rotating Luer lock connection according to the applicable equipment instructions.
- Route the tubing to avoid kinking, compression, excessive tension, or interference with the sterile field.
- Confirm that the tubing pathway is unobstructed before initiating insufflation.
- Operate the insufflator according to the equipment manufacturer's recommended pressure and flow settings.
- Monitor the tubing and connection points during the procedure for disconnection, obstruction, kinking, or other performance concerns.
- Dispose of the single-use tubing according to institutional procedures after the procedure.
Healthcare professionals should consult current manufacturer instructions for complete setup, compatibility, warnings, contraindications, storage, handling, and disposal requirements.
Certifications and Safety Standards
The BD LA101-RLL is intended for professional surgical use and should be incorporated into established medical device safety, infection-prevention, and operating room equipment protocols.
The tubing is supplied sterile and includes a bidirectional 0.1-micron hydrophobic filter designed to help reduce the chance of contamination. The product is also not made with natural rubber latex, supporting healthcare facilities that maintain product-selection policies related to latex exposure.
The filtration system should be used as designed and should not be bypassed, removed, modified, or substituted with an unapproved component. Proper connection, equipment compatibility, package inspection, and adherence to manufacturer instructions remain essential for safe use.
Healthcare facilities and procurement teams should verify current manufacturer documentation for applicable regulatory status, UDI information, sterilization details, expiration dating, material specifications, and other product-specific requirements.
Comparison with Competitors
Compared with insufflation tubing that uses a larger-pore filter, the BD LA101-RLL incorporates a 0.1-micron hydrophobic filter for facilities and procedures requiring this specific filtration configuration. Product selection should be based on compatible equipment, procedural requirements, and manufacturer recommendations.
Compared with fixed Luer connections, the rotating Luer lock configuration can provide greater flexibility during setup by allowing rotational movement at the connection point and helping reduce unwanted tubing twist.
Compared with reusable insufflation tubing, the single-use BD LA101-RLL eliminates the need to clean, inspect, and reprocess the tubing between procedures. This can simplify workflow while supporting standardized single-use practices.
Competing insufflation tubing products may vary in filter pore size, flow characteristics, connector design, tubing length, sterility, material composition, and equipment compatibility. The BD LA101-RLL combines a 0.1-micron hydrophobic filter, rotating Luer lock connection, 10-foot tubing length, sterile single-use design, and 20-per-box packaging for professional laparoscopic applications.
Typical User Profile and Application Scenarios
The BD LA101-RLL Insufflation Tubing is intended for trained healthcare professionals involved in laparoscopic and minimally invasive surgical procedures. Typical users may include surgeons, operating room nurses, surgical technologists, and other qualified clinical personnel responsible for surgical equipment setup and intraoperative support.
Typical application scenarios include procedures requiring a connection between a compatible insufflator and laparoscopic access system for controlled gas delivery. The 10-foot tubing length can be particularly useful in operating rooms where equipment positioning requires additional distance between the insufflator and procedural field.
The product is well suited for hospitals, operating rooms, ambulatory surgery centers, and specialty surgical facilities that routinely perform laparoscopic procedures and require sterile, single-use insufflation tubing.
Best Practices for Use and Maintenance
The BD LA101-RLL is a sterile, single-use procedural product and should be stored, handled, used, and disposed of according to current manufacturer labeling and healthcare facility procedures. It is not intended to be maintained or reprocessed as reusable equipment.
- Store unopened products according to manufacturer-recommended environmental conditions.
- Protect sterile packaging from moisture, contamination, excessive heat, crushing, and physical damage.
- Rotate inventory according to expiration dates when applicable.
- Verify the correct catalog number and equipment compatibility before opening the package.
- Inspect the tubing, filter, connector, and sterile barrier before use.
- Avoid sharp bends, kinks, compression, and excessive tension along the tubing pathway.
- Keep the tubing positioned to minimize interference with staff movement and surgical equipment.
- Confirm that all connections remain secure throughout the procedure.
- Do not cut, modify, bypass, or remove the integrated filter or connector components.
- Do not reuse or reprocess the single-use tubing.
- Dispose of the product according to applicable infection-control and medical waste procedures.
Regulatory and Safety Information
The BD LA101-RLL Insufflation Tubing should be used only by appropriately trained healthcare professionals and only with compatible insufflation equipment. The product should be incorporated into established surgical safety, equipment inspection, and infection-prevention procedures.
Before use, verify the product identity, sterile package integrity, tubing condition, filter integrity, connector compatibility, and suitability for the intended procedure. Kinked tubing, obstruction, improper connection, or incompatible equipment may affect insufflation performance.
Insufflation pressure and flow should be controlled through the compatible insufflator and managed according to equipment instructions, procedural requirements, and professional clinical judgment. The tubing does not replace appropriate pressure monitoring or insufflator safety systems.
The integrated 0.1-micron hydrophobic filter should remain intact throughout use. It should not be removed, bypassed, or altered. The product is intended for single use and should not be reused or reprocessed after the procedure.
Specific FDA status, UDI information, sterilization method, expiration requirements, and other regulatory characteristics should be confirmed from current manufacturer documentation when required for purchasing, facility approval, or clinical use.
How to Order
Select the BD LA101-RLL - Insufflation Tubing, Rotating Luer Lock, 0.1 Micron Filter, 10 ft and add it to your cart. Complete checkout with your preferred shipping and payment options. For bulk orders, quotes, or further assistance, contact CIA Medical customer service at (312)275-5850 or use the contact form on this page.
