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BD CH112 - Vascular Maxi Loop, Yellow, 0.10" x 14.75" x 0.04", Radiopaque Silicone, Sterile, 10/BX (Temp Sensitive; Non-Returnable) (Continental US Only)

BD  # CH112 - Vascular Maxi Loop, Yellow, 0.10
Part Number BD CH112
SKU Number CIA8042446
Sell Unit BOX
Ships Within Special Order
List Price $123.62
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Product Description

BD CH112 - Vascular Maxi Loop, Yellow, 0.10" x 14.75" x 0.04", Radiopaque Silicone, Sterile, 10/BX (Temp Sensitive; Non-Returnable) (Continental US Only)

The BD CH112 Vascular Maxi Loop is a sterile, single-use surgical loop designed to support the identification, retraction, occlusion, and temporary control of anatomical structures during vascular and other surgical procedures. The yellow Maxi loop measures 0.10 inch wide by 14.75 inches long by 0.04 inch deep, or approximately 2.5 mm x 375 mm x 1 mm, providing a flexible profile for controlled surgical handling.

Made from medical-grade radiopaque silicone, the BD CH112 is suitable for use with arteries, veins, tendons, nerves, and other appropriate anatomical structures. Its flexible silicone construction allows the loop to conform around anatomical structures, while the yellow color provides clear visual differentiation within the operative field.

The radiopaque material provides an additional identification feature during surgical procedures. Its sterile, single-use configuration supports established infection-control and operating room protocols. The product is not made with natural rubber latex and is packaged two loops per pack with 10 packs per box.

Key Benefits

  • Maxi-size vascular loop supports identification, retraction, occlusion, and temporary control of appropriate anatomical structures.
  • Yellow color provides clear visual contrast and supports differentiation within the operative field.
  • Medical-grade silicone construction provides flexibility for controlled surgical placement.
  • Radiopaque material supports identification when radiographic detection is clinically required.
  • Suitable for use with arteries, veins, tendons, nerves, and other appropriate structures.
  • Sterile presentation supports established aseptic surgical workflows.
  • Single-use design eliminates the need for cleaning and reprocessing between procedures.
  • Not made with natural rubber latex for facilities managing latex-related product requirements.
  • Long 14.75-inch configuration provides ample length for positioning and handling during surgery.

Compatibility and Applications

The BD CH112 Vascular Maxi Loop is designed for integration into vascular, general, orthopedic, and other surgical workflows requiring temporary identification, isolation, retraction, occlusion, or control of anatomical structures.

Typical applications may include identifying arteries and veins, retracting vessels or surrounding structures from the operative field, temporarily controlling vascular structures, and differentiating tendons or nerves during appropriate procedures.

The Maxi configuration provides a larger profile than Mini vascular loop options and may be selected when increased visibility or a more substantial loop is appropriate. Product selection should reflect the anatomical structure, surgical technique, clinician preference, and current manufacturer instructions.

The BD CH112 is suitable for hospital operating rooms, ambulatory surgery centers, vascular surgery departments, specialty surgical facilities, and other controlled procedural environments. It may be used with compatible surgical instruments and accepted vessel-management techniques when clinically appropriate.

Usage Guidelines

Before use, confirm the BD CH112 catalog number, yellow color, Maxi dimensions, sterile package integrity, expiration information when applicable, and suitability for the intended surgical procedure.

  • Use appropriate aseptic technique when opening the package and introducing the vascular loop into the sterile field.
  • Select the loop only when the Maxi size is appropriate for the anatomical structure and intended technique.
  • Position the loop carefully around the intended vessel, tendon, nerve, or other structure.
  • Apply only the amount of tension necessary for identification, retraction, occlusion, or temporary control.
  • Avoid excessive tension that could compress, damage, or traumatize delicate tissue.
  • Maintain clear visual identification of the yellow loop throughout the procedure.
  • Account for every surgical loop introduced into the operative field according to institutional protocols.
  • Dispose of the loop after use according to applicable infection-control and medical waste requirements.

Healthcare professionals should consult current manufacturer labeling and institutional surgical protocols for complete handling instructions, warnings, contraindications, and disposal requirements.

Certifications and Safety Standards

The BD CH112 Vascular Maxi Loop is intended for professional surgical use and should be handled in accordance with applicable medical device regulations, infection-prevention procedures, surgical safety protocols, and current manufacturer instructions.

The product is supplied sterile and is intended for single use. Maintaining sterile package integrity and using appropriate aseptic technique are essential for preserving the product's condition before use.

The medical-grade radiopaque silicone construction provides an additional identification feature when radiographic detection is clinically necessary. Radiopacity should complement established surgical item accountability procedures rather than replace manual counts, visual inspection, or count reconciliation.

The product is not made with natural rubber latex. Healthcare facilities and procurement teams should verify current manufacturer documentation for applicable regulatory status, UDI information, sterilization details, expiration dating, and other product-specific requirements.

Comparison with Competitors

Compared with Mini vascular loops, the BD CH112 Maxi Loop provides a larger 0.10-inch width and 0.04-inch depth. This larger profile may be preferred when greater visibility or a more substantial loop configuration is required during the procedure.

Compared with non-radiopaque vessel loops, the radiopaque silicone construction provides an additional detection feature that may support surgical safety procedures when radiographic identification is required.

Compared with reusable vessel-control accessories, the sterile single-use design eliminates the need for cleaning, inspection, and reprocessing between procedures. This can simplify procedural preparation and support standardized single-use practices.

Competing vascular loops may vary in size, color, material, radiopacity, sterility, and packaging configuration. The BD CH112 combines a yellow Maxi profile, medical-grade radiopaque silicone, sterile single-use presentation, and a 14.75-inch length for professional surgical applications.

Typical User Profile and Application Scenarios

The BD CH112 Vascular Maxi Loop is intended for trained healthcare professionals involved in vascular and other surgical procedures. Typical users may include vascular surgeons, general surgeons, orthopedic surgeons, physicians, operating room nurses, surgical technologists, and other qualified clinical personnel.

Typical application scenarios include procedures requiring temporary vessel control, identification of arteries or veins, retraction of anatomical structures, and visual differentiation of tendons or nerves during surgery.

The yellow color may be incorporated into a surgeon's or healthcare facility's color-based identification system when multiple structures or loops are used. The meaning assigned to each loop color should remain consistent and clearly understood by the surgical team.

The product is particularly relevant for hospitals, operating rooms, ambulatory surgery centers, vascular surgery facilities, and other healthcare environments requiring sterile, single-use surgical accessories.

Best Practices for Use and Maintenance

The BD CH112 is a sterile, single-use surgical 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 under the environmental conditions recommended by the manufacturer.
  • 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, yellow color, and Maxi configuration before opening the package.
  • Inspect the sterile barrier and loop condition before use.
  • Do not cut, modify, excessively stretch, or otherwise alter the loop.
  • Use only the amount of tension required for the intended surgical purpose.
  • Maintain accountability for all loops introduced into the operative field.
  • Do not reuse or reprocess the single-use product.
  • Dispose of used loops according to applicable infection-control and regulated medical waste procedures.

Regulatory and Safety Information

The BD CH112 Vascular Maxi Loop should be used only by appropriately trained healthcare professionals and only for applications consistent with current manufacturer labeling, professional clinical judgment, and institutional policy.

Before use, verify the product identity, dimensions, yellow color, sterile package integrity, expiration information when applicable, and suitability for the intended procedure. Do not use a product that is damaged, contaminated, expired, or supplied in compromised packaging.

Excessive tension or inappropriate application may damage delicate anatomical structures. The loop should be positioned and manipulated using accepted surgical techniques and only under the direction of a qualified healthcare professional.

The product is made from medical-grade radiopaque silicone, supplied sterile, intended for single use, and not made with natural rubber latex. Every vascular loop introduced into the operative field should be managed according to applicable surgical item accountability procedures.

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 CH112 - Vascular Maxi Loop, Yellow, Single Use, Sterile 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.

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