BD 23275-650 - Tonsil Sponge, ", Unstrung, Cotton, X-Ray Detectable, 5/PK, 50 PK/CS (Temp Sensitive; Non-Returnable)

BD 23275-650 - Tonsil Sponge, ", Unstrung, Cotton, X-Ray Detectable, 5/PK, 50 PK/CS (Temp Sensitive; Non-Returnable)

The BD 23275-650 Tonsil Sponge is a compact surgical sponge designed for effective fluid absorption, surgical preparation, localized packing, and procedural site management. Measuring inch, or 1.9 cm, the sponge features an unstrung configuration and cotton construction that provide a highly absorbent solution for appropriate surgical and clinical applications.

The small -inch profile supports controlled placement in confined procedural areas where a larger surgical sponge may be less suitable. Its cotton construction provides excellent absorbency for blood, preparation solutions, and other procedural fluids, helping healthcare professionals maintain a clearer and more manageable surgical field.

The BD 23275-650 is X-ray detectable, providing an additional safety feature for surgical environments where sponge accountability is essential. The unstrung design offers a streamlined configuration for procedures where a retrieval string is not required. The product is packaged five sponges per pack and 50 packs per case, providing a total of 250 sponges for hospitals, operating rooms, ambulatory surgery centers, and specialty surgical facilities.

Key Benefits

• Compact -inch size supports precise placement in confined surgical and procedural areas.
• Cotton construction provides excellent absorbency for blood and other procedural fluids.
• Unstrung configuration offers a streamlined sponge profile for appropriate surgical applications.
• X-ray detectable construction supports retained surgical item prevention protocols.
• Suitable for use as a preparation sponge during appropriate surgical procedures.
• Helps maintain a clearer operative field through effective localized fluid absorption.
• Small size provides an alternative to larger tonsil and conventional gauze sponges.
• Five sponges per pack support organized procedural preparation and inventory control.
• Fifty packs per case provide 250 sponges for efficient institutional supply management.

Compatibility and Applications

The BD 23275-650 Tonsil Sponge is designed for integration into established surgical and procedural workflows. It may be used with appropriate surgical forceps, clamps, sponge-holding instruments, and other compatible instruments when instrument-assisted placement or manipulation is clinically indicated.

Typical applications may include tonsil and adenoid procedures, oral and pharyngeal surgery, surgical site preparation, localized fluid absorption, cavity packing, and other procedures requiring a compact absorbent cotton sponge.

The product is suitable for hospital operating rooms, ambulatory surgery centers, ENT surgical departments, specialty surgical facilities, and other controlled healthcare environments. Healthcare professionals should confirm that the -inch unstrung configuration is appropriate for the specific procedure before use.

Usage Guidelines

Before use, confirm the BD 23275-650 catalog number, -inch size, unstrung configuration, package integrity, and suitability for the intended procedure. Healthcare professionals should follow current manufacturer instructions and institutional procedures throughout preparation, use, accountability, and disposal.

• Select the sponge only when its -inch unstrung configuration is appropriate for the intended procedure.
• Inspect the packaging before use and do not use products from damaged or compromised packaging.
• Use appropriate aseptic technique whenever the sponge is introduced into a controlled surgical field.
• Use compatible surgical instruments when instrument-assisted placement or manipulation is required.
• Apply only the pressure necessary for fluid absorption, packing, or procedural site management.
• Follow established sponge count procedures before, during, and after the surgical procedure.
• Account for every sponge introduced into the operative field before completing the procedure.
• Dispose of used sponges according to institutional infection-control and regulated medical waste procedures.

Healthcare professionals should review current manufacturer labeling and applicable facility protocols for complete product-specific handling, storage, warning, and disposal information.

Certifications and Safety Standards

The BD 23275-650 Tonsil Sponge is intended for professional healthcare use and should be handled in accordance with applicable medical device regulations, infection-control procedures, surgical safety protocols, and current manufacturer documentation.

The X-ray detectable design provides an additional safety feature for surgical environments by supporting identification procedures when clinically required. X-ray detectability should complement established visual inspection, manual sponge counting, count reconciliation, and retained surgical item prevention procedures.

Healthcare facilities and procurement teams should verify current manufacturer documentation for applicable regulatory information, UDI data, package status, expiration dating, material specifications, latex information, sterilization details when applicable, and market-specific requirements.

Comparison with Competitors

Compared with conventional flat gauze sponges, the BD 23275-650 Tonsil Sponge provides a smaller and more focused profile for localized fluid absorption, preparation, and procedural site management. Standard gauze sponges are generally better suited for broad surface coverage, while a compact tonsil sponge can provide greater control in confined surgical areas.

Compared with double-strung tonsil sponges, the unstrung BD 23275-650 offers a streamlined configuration without external retrieval strings. This may be preferred for procedures where an unstrung sponge is specifically selected, although it requires strict adherence to established sponge accountability and retained surgical item prevention protocols.

Compared with medium and large tonsil sponge configurations, the -inch size provides a smaller working profile for procedures requiring precise placement. Similar competitor products may vary in dimensions, absorbency, material, string configuration, X-ray detectability, and packaging quantity.

The BD 23275-650 combines a compact -inch size, absorbent cotton construction, unstrung design, X-ray detectability, and organized institutional packaging for professional surgical use.

Typical User Profile and Application Scenarios

The BD 23275-650 Tonsil Sponge is intended for use by trained healthcare professionals involved in surgical and procedural care. Typical users may include otolaryngologists, ENT surgeons, general surgeons, physicians, operating room nurses, surgical technologists, and other qualified clinical personnel.

Typical application scenarios include tonsil and adenoid procedures, oral and pharyngeal surgery, localized cavity packing, surgical preparation, fluid absorption, and maintenance of a clear operative field.

The compact -inch configuration is particularly relevant when precise placement is required within a confined procedural area. The product is well suited for hospitals, operating rooms, ambulatory surgery centers, ENT surgical facilities, and other healthcare environments that require dependable absorbent surgical supplies and formal sponge-accountability procedures.

Best Practices for Use and Maintenance

The BD 23275-650 is a surgical consumable 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 as reusable surgical equipment.

• Store unopened products according to environmental conditions recommended by the manufacturer.
• Protect packaging from moisture, contamination, excessive heat, crushing, and physical damage.
• Rotate inventory according to expiration dates when expiration dating is provided.
• Verify the correct catalog number, -inch size, and unstrung configuration before use.
• Inspect the package before introducing the product into a procedural environment.
• Maintain accurate sponge counts throughout the procedure.
• Exercise particular care with unstrung sponges because no retrieval string is present.
• Do not rely solely on X-ray detectability as a replacement for established counting protocols.
• Do not reuse or reprocess the product when designated for single use.
• Dispose of used products according to applicable infection-control and medical waste requirements.

Regulatory and Safety Information

The BD 23275-650 Tonsil Sponge 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, -inch size, unstrung configuration, package condition, expiration information when applicable, and suitability for the intended procedure.

Every sponge introduced into an operative field should be incorporated into the healthcare facility's established surgical item counting and retained item prevention procedures. Because the BD 23275-650 is unstrung, careful sponge accountability is particularly important. X-ray detectability provides an additional identification feature when clinically necessary but does not replace manual counting, visual inspection, count reconciliation, or other established surgical safety protocols.

Specific FDA status, UDI information, sterilization details, material information, latex status, 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 23275-650 - Tonsil Sponge, Unstrung, " 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.