Medical Suction Pouch 1.5L - 1500ccm (x50) - Cardinal Health (65651920) - Delynov

What is the Cardinal Health 1.5L medical suction liner?

The 1.5L medical suction liner, referenced under code 65651920 by Cardinal Health, is a collection device designed for the recovery of fluids in a surgical environment. Presented in a 1500ccm format, it is specifically developed by Cardinal Health Inc. to meet biological liquid management needs. This operating room consumable allows for the secure collection of effluents. Its design is adapted to suction systems used in oral surgery practices and hospital environments, offering a temporary storage solution for fluids aspirated during the operative act. The packaging in lots of 50 units allows for constant availability for practitioners performing regular interventions.

What are the clinical indications for this surgical suction liner?

This surgical suction liner is indicated for the collection of blood, saliva, and irrigation solutions (saline solution) during various interventions. In oral surgery, it is used during implant placement, complex extractions, sinus lifts, or bone grafts. The clinical objective is to maintain optimal visibility of the operative site by evacuating liquids that could hinder the practitioner. The 1.5l suction liner offers sufficient capacity for medium to long duration surgeries, ensuring that the suction process is not interrupted by premature filling of the container. It is an essential component of the surgical suction chain to ensure hygiene and the smooth progress of care.

What are the technical characteristics of this Cardinal Health device?

The Cardinal Health suction liner features precise technical specifications for the operating room. Its nominal capacity is 1500ccm, or 1.5L, which corresponds to the standards for maxillofacial and oral surgery interventions. The product is identified by the manufacturer reference 65651920. Its structure is designed to resist the negative pressure exerted by suction pumps without collapsing, guaranteeing a constant collection volume. Although the exact composition is not specified, these devices are generally manufactured from resistant polymers allowing for visualization of the filling level. The connection system is designed to fit standard liquid collection tubing, ensuring the seal necessary for the biological safety of the practice.

What are the contraindications for the use of this product?

There are no specific documented medical contraindications for the use of a liquid collection liner, as the device does not come into direct contact with the patient. However, use is strictly limited to the collection of aspirated fluids. It must not be used to store chemical substances incompatible with polymer materials or for liquids intended to be reinjected. The practitioner must ensure the compatibility of the liner with the support canister and the centralized or mobile suction system used. Improper installation could lead to a loss of vacuum, compromising the effectiveness of the surgical suction. One should systematically refer to the instructions for use provided by Cardinal Health Inc. to guarantee compliant usage.

What are the precautions for use and post-intervention processing?

As a device in the CONSO (consumable) category, this suction liner is intended for single use. After each oral surgery intervention, the liner must be removed, hermetically sealed, and disposed of according to the protocol for treating Infectious Risk Healthcare Activity Waste (DASRI). Never attempt to empty, clean, or resterilize a used liner, as this would present a major risk of cross-contamination for staff and subsequent patients. Systematic replacement between two patients is imperative. Before use, healthcare personnel must check the integrity of the packaging and the liner to ensure that no perforation alters the seal of the suction circuit.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Cardinal Health Inc., a globally recognized player in the supply of medical and surgical products. The brand Cardinal Health ensures the traceability of this reference 65651920. Regarding regulatory certifications such as the risk class or specific CE marking, this information is not detailed in the current technical documentation of the product. However, as a medical device manufacturer, Cardinal Health designs its products according to rigorous quality processes. Practitioners are invited to consult the product labeling and the technical notice attached to each box of 50 units to verify the regulatory compliances in force at the time of purchase, in accordance with the requirements of their healthcare facility.

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Surgical medical consumables play a decisive role in operative safety.