1.5 liter polycarbonate urine collection system for dental surgery - Medela (077.0082) - Delynov

What is the Medela 1.5 litres polycarbonate jar?

The 1.5 litres polycarbonate jar for urine collector systems, distributed under the brand Medela France, is a robust collection device intended for the medical environment. This medical polycarbonate jar is specifically designed by the manufacturer Medela to offer a reliable and secure fluid storage solution. Its polycarbonate structure provides increased impact resistance and the transparency necessary for visual monitoring of collected volumes. This surgical suction jar, bearing reference 077.0082, is a central element of suction systems used by healthcare professionals for the management of liquid effluents during surgical procedures or intensive care.

What are the clinical indications?

This surgical suction jar is indicated for the collection of body fluids, particularly within the framework of urine collector systems or during various surgical aspirations. Its use is strictly reserved for trained healthcare professionals. The Medela France device allows for the hygienic collection of secretions, thus preventing contamination of the care environment. In surgery or follow-up care, this surgical suction reservoir is used to quantify and isolate aspirated biological liquids. It is imperative to read the instructions carefully before any commissioning to guarantee use in accordance with the clinical protocols in force in healthcare establishments.

What are the technical characteristics?

The polycarbonate suction jar presents precise technical characteristics under reference 077.0082. It has a capacity of 1.5 litres, offering an intermediate storage volume suitable for many clinical procedures. Manufactured from polycarbonate, a polymer recognized for its strength, this Medela France surgical suction jar guarantees optimal durability against daily handling. Its design allows for fluid integration with accessories from the Medela range to constitute a complete suction system. The manufacturer specifies that the equipment must be used in accordance with the instructions provided, respecting the instructions for use included in the packages to ensure the tightness and proper functioning of the collection system.

What are the contraindications for use?

The manufacturer does not list specific medical contraindications for this polycarbonate jar in the technical documentation provided. However, the use of this device is exclusively reserved for healthcare professionals. Improper handling or use outside the scope intended by the manufacturer Medela could compromise the safety of the patient or the operator. It is essential to follow the instructions in our user manuals included in the packages of each product to avoid any risk related to incorrect installation. Failure to comply with cleaning or sterilization protocols, if applicable, could constitute an indirect contraindication to its safe reuse.

What are the precautions for use and maintenance?

For the use of this medical polycarbonate jar, the precautions for use dictated by the manufacturer Medela must be scrupulously followed. Healthcare professionals are reminded to read the manual carefully before use. Warnings and precautions include strict adherence to the instructions in our user manuals included in the packages of each product. As it is a Class I device, it requires careful handling to maintain the integrity of the polycarbonate. The absence of cracks or damage on the jar should be checked before each use to guarantee the tightness of the suction system. Storage must be carried out according to recommendations to preserve the mechanical properties of the material.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Medela, located at Lättichstrasse 4B, 6340 Baar, Switzerland. This product is classified as a Class I medical device according to current regulations. Compliance with manufacturing standards is ensured by the recognized manufacturer Medela, guaranteeing the quality of the surgical suction jar under reference 077.0082. As a Class I product, it meets the safety and performance requirements for equipment intended for healthcare professionals. Traceability and compliance are documented under revision G2S 011634 0169 Rev. 02. Users must systematically refer to the official technical documentation for any information relating to specific certifications not detailed here.

State of the art

Surgical medical consumables play a decisive role in operative safety.