BD 23275-660 - Tonsil Sponge, 1 ", Unstrung, Cotton, Sterile, X-Ray Detectable, 5/PK, 50 PK/CS (Temp Sensitive; Non-Returnable)

BD 23275-660 - Tonsil Sponge, 1 ", Unstrung, Cotton, Sterile, X-Ray Detectable, 5/PK, 50 PK/CS (Temp Sensitive; Non-Returnable)

The BD 23275-660 Tonsil Sponge is a sterile, unstrung surgical sponge designed for effective fluid absorption, surgical preparation, localized packing, and procedural site management. Measuring 1 inches, or 3.2 cm, the sponge features absorbent cotton construction and a larger profile for procedures requiring greater surface area and fluid capacity than smaller tonsil sponge configurations.

The unstrung design provides a streamlined sponge profile for surgical applications where a retrieval string is not required. Its absorbent cotton construction helps manage blood, preparation solutions, and other procedural fluids while supporting a clearer and more controlled operative field.

The BD 23275-660 is X-ray detectable, providing an additional safety feature for retained surgical item prevention protocols. It 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

• Large 1 -inch size provides an effective absorbent surface for surgical preparation and fluid management.
• Cotton construction offers reliable absorption of blood and other procedural fluids.
• Unstrung configuration provides a streamlined profile for appropriate surgical applications.
• Sterile presentation supports aseptic surgical technique and infection-control protocols.
• X-ray detectable construction supports retained surgical item prevention procedures.
• Suitable for localized packing, surgical preparation, and procedural site management.
• Larger size provides greater surface area than smaller tonsil sponge configurations.
• 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 23275-660 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 larger 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 1 -inch unstrung configuration is appropriate for the specific procedure before use.

Usage Guidelines

Before use, confirm the BD 23275-660 catalog number, 1 -inch size, unstrung configuration, sterile package integrity, and suitability for the intended procedure. Do not use the product if the sterile packaging is opened, damaged, wet, punctured, or otherwise compromised.

• Use appropriate aseptic technique when opening the package and introducing the sponge into the sterile field.
• Select the sponge only when its 1 -inch unstrung configuration is appropriate for the intended procedure.
• 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 23275-660 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 sterile presentation supports use in controlled surgical environments when package integrity and proper aseptic technique are maintained. The X-ray detectable design provides an additional identification feature for surgical safety protocols and retained surgical item prevention procedures.

X-ray detectability should complement established visual inspection, manual sponge counting, count reconciliation, and other institutional safety procedures. It should not be considered a replacement for standard surgical item accountability practices.

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

Comparison with Competitors

Compared with conventional flat gauze sponges, the BD 23275-660 Tonsil Sponge provides a more compact and specialized profile for localized packing, fluid absorption, and surgical site preparation. Standard gauze sponges are generally better suited for broad surface coverage, while a tonsil sponge can provide more controlled placement in confined surgical areas.

Compared with the smaller -inch unstrung tonsil sponge configuration, the BD 23275-660 offers a larger 1 -inch profile with greater surface area for procedures requiring increased absorbent capacity or broader contact within the surgical field.

Compared with double-strung alternatives, the unstrung BD 23275-660 provides a streamlined configuration without external retrieval strings. This may be preferred for procedures where an unstrung sponge is specifically selected, although strict adherence to sponge counting and retained surgical item prevention procedures remains essential.

Similar competitor products may vary in dimensions, absorbency, cotton construction, string configuration, sterility, X-ray detectability, and packaging quantity. The BD 23275-660 combines a large 1 -inch size, absorbent cotton construction, sterile presentation, unstrung design, and X-ray detectability for professional surgical use.

Typical User Profile and Application Scenarios

The BD 23275-660 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 larger 1 -inch configuration is particularly relevant when greater sponge surface area or absorbent capacity is required. The product is well suited for hospitals, operating rooms, ambulatory surgery centers, ENT surgical facilities, and other healthcare environments that require sterile surgical supplies and formal sponge-accountability procedures.

Best Practices for Use and Maintenance

The BD 23275-660 is a sterile 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 sterile 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, 1 -inch size, and unstrung configuration before use.
• Inspect the sterile barrier before opening the product.
• 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 23275-660 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, 1 -inch size, unstrung configuration, sterile package integrity, 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 23275-660 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 method, material details, latex information, 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 23275-660 - Tonsil Sponge, Unstrung, 1 " 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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