BD 23276-250 - Cylindrical Sponge, " x 1 ", Unstrung Surgical Sponge, 50/CS (Temp Sensitive; Non-Returnable)
The BD 23276-250 Cylindrical Sponge is a compact, unstrung medical sponge measuring inch by 1 inches. Its cylindrical configuration is designed to support controlled handling in surgical and clinical procedures where a small, absorbent sponge is required for localized fluid management, tissue contact, or procedural assistance.
The compact shape allows healthcare professionals to work within confined or targeted procedural areas while maintaining greater control than may be possible with larger flat gauze sponges. Depending on the procedure and the manufacturer's instructions for use, cylindrical sponges may be used to absorb blood and other fluids, support wound or procedural site management, assist with gentle tissue manipulation, or apply an appropriate topical solution.
This product is not intended to function as an intravenous fluid or medication delivery device. Any use involving topical solutions, medications, tissue contact, or surgical procedures should follow the manufacturer's labeling, facility protocols, and the direction of a qualified healthcare professional.
Key Benefits
- Compact " x 1 " cylindrical design supports precise placement in localized procedural areas.
- Absorbent sponge construction assists with management of blood and other fluids during appropriate clinical procedures.
- Unstrung configuration provides a streamlined profile for applications where a retrieval string is not preferred.
- Small cylindrical shape can provide greater access and control in confined areas than larger conventional gauze sponges.
- Suitable for integration into established surgical and clinical workflows when the product specifications match the procedural requirements.
- Supports efficient procedural site management by helping clinicians maintain visibility and control of localized fluids.
Compatibility and Applications
The BD 23276-250 Cylindrical Sponge is intended for use as a procedural consumable rather than as a component that mechanically connects to another medical device. It may be used with compatible surgical instruments and standard clinical techniques when directed by the healthcare professional and permitted by the manufacturer's instructions.
Potential applications may include surgical procedures, outpatient procedures, specialty care, procedural site fluid absorption, gentle tissue handling, and other situations in which a small cylindrical sponge is clinically appropriate. Typical environments may include hospital operating rooms, ambulatory surgery centers, specialty clinics, and other controlled healthcare settings.
Before use with forceps, clamps, applicators, or other instruments, clinicians should confirm that the selected handling method is appropriate for the sponge and procedure. Do not assume compatibility with a specific instrument, surgical technique, or anatomical application unless supported by current product labeling and institutional protocol.
Usage Guidelines
Review the current product label and manufacturer's instructions before use. Confirm the catalog number, dimensions, package integrity, expiration information when applicable, and any stated sterility or single-use designation before introducing the product into a clinical field.
- Select the sponge only when its " x 1 " size and unstrung configuration are appropriate for the intended procedure.
- Inspect the packaging and product before use. Do not use a product from packaging that is damaged, compromised, wet, or otherwise unsuitable.
- Use aseptic technique whenever the product is supplied for use in a sterile field.
- Handle the sponge with an appropriate technique and compatible instrument when instrument-assisted placement or removal is required.
- Follow the facility's sponge accounting, procedural count, and retrieval protocols when the product is used during surgery.
- Dispose of used products according to applicable facility procedures and regulations for contaminated medical waste.
Healthcare facilities should refer to current manufacturer documentation for definitive instructions, warnings, contraindications, storage requirements, and product-specific procedural guidance.
Certifications and Safety Standards
Healthcare products should be purchased and used according to the regulatory requirements applicable to the destination market and the healthcare facility. Product-specific regulatory status, sterility claims, UDI information, material specifications, latex status, and other certifications should be confirmed from the current manufacturer labeling and documentation associated with BD 23276-250.
Buyers should not assume FDA clearance, CE marking, x-ray detectability, radiopacity, or a particular sterilization method unless the specific claim appears on the current product label or supporting manufacturer documentation. Maintaining this verification process helps healthcare organizations align procurement decisions with internal quality systems, infection-control procedures, and applicable regulatory requirements.
Comparison with Competitors
Compared with conventional flat gauze sponges, the BD 23276-250 offers a compact cylindrical profile that may provide more controlled placement in smaller or confined procedural areas. Flat gauze products are often preferred for broad surface absorption, while cylindrical sponges are better suited to applications requiring a smaller, more focused sponge format.
Compared with peanut dissectors and other specialty surgical sponges, the " x 1 " dimensions provide a distinct size option for clinicians selecting a sponge according to procedural requirements. Product selection should consider absorbency, shape, dimensions, handling characteristics, sterility, detectability requirements, and the specific surgical technique.
The unstrung configuration distinguishes the BD 23276-250 from strung sponge alternatives. An unstrung sponge may provide a less obstructive profile during use, while strung alternatives may be preferred when a retrieval string is required by the procedure or facility protocol. Because the BD 23276-250 is specified as unstrung, strict adherence to institutional sponge management and accounting procedures is particularly important when used in operative settings.
Typical User Profile and Application Scenarios
The BD 23276-250 Cylindrical Sponge is primarily intended for use by trained healthcare professionals who require a compact procedural sponge. Typical users may include surgeons, physicians, nurses, surgical technologists, operating room personnel, and other appropriately trained clinical staff.
Common application scenarios may include procedures in which localized fluid absorption, controlled sponge placement, or gentle procedural site management is required. The product may be particularly relevant in operating rooms, ambulatory surgery centers, specialty procedure rooms, and clinical environments where the " x 1 " cylindrical format is specifically selected for the procedure.
Best Practices for Use and Maintenance
As a medical sponge, the BD 23276-250 should be managed according to its package labeling rather than maintained as reusable equipment. Proper storage, handling, inspection, and disposal are essential to preserving product integrity and supporting safe clinical use.
- Store unopened product in accordance with the manufacturer's recommended environmental conditions.
- Protect packaging from moisture, excessive heat, contamination, crushing, and physical damage.
- Rotate inventory according to expiration dates when expiration dating is provided.
- Confirm the correct catalog number and sponge size before opening the package.
- Do not reuse or reprocess the product when it is labeled for single use.
- Do not alter, cut, attach a string to, or otherwise modify the sponge unless specifically permitted by the manufacturer.
- Use established sponge count and retrieval procedures in surgical environments.
- Do not assume that the sponge is x-ray detectable unless this characteristic is expressly confirmed on the applicable product packaging.
Regulatory and Safety Information
The BD 23276-250 should be used only by appropriately trained personnel and for applications consistent with current manufacturer labeling and institutional policy. Before use, confirm the product identity, package condition, dimensions, and all relevant labeling information.
When used in a surgical setting, healthcare facilities should apply their established policies for sponge counts, prevention of retained surgical items, aseptic technique, infection control, and post-procedure disposal. Because this product is described as unstrung, users should pay particular attention to procedural accountability and retrieval practices.
Specific regulatory approvals and compliance documentation may vary by market, product configuration, and current manufacturer registration status. Procurement teams should review the latest manufacturer documentation when FDA status, UDI information, CE marking, sterility validation, material composition, latex information, or other regulatory characteristics are required for purchasing or clinical approval.
How to Order
Select the BD 23276-250 - Cylindrical Sponge, " x 1 ", 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.
