1 case of 9 boxes of 200 self-adhesive sterilization pouches 75 x 250 mm (x1800 units) - MEDI STOCK (E5017) - Delynov

What is the carton of 1800 MEDI STOCK sterilization pouches (E5017)?

This product, offered under the brand MEDI STOCK, is a packaging set for steam sterilization. It consists of a main carton containing 9 boxes of 200 units, for a total of 1800 pouches. Each sterilization pouch has dimensions of 75 x 250 mm, a size suitable for receiving various surgical instruments. The structure of the pouch is designed to allow the penetration of the sterilizing agent while constituting an effective microbiological barrier after treatment. The self-adhesive closure system simplifies equipment preparation in oral surgery practices by avoiding the use of a separate thermal sealer.

What are the clinical indications for these pouches?

In clinical practice, particularly in implantology or periodontology, these pouches are indicated for the packaging of instrumentation that must undergo a sterilization cycle. They allow for the grouping of specific instruments by procedure kit or the protection of individual devices. The use of the dental sterilization pouch is systematic before any invasive procedure to guarantee the asepsis of the operating field. They are particularly useful for packaging mirrors, probes, tweezers, or forceps of standard size, ensuring that each device remains protected from any environmental contamination until it is opened at the chairside during the surgical act.

What are the technical characteristics of reference E5017?

Reference E5017 from the brand MEDI STOCK is distinguished by its 75 x 250 mm format. This length of 250 mm is ideal for thin but long instruments. The product is manufactured to withstand the physical constraints of autoclave cycles. Each pouch is equipped with an adhesive strip protected by a removable film, allowing for a fast and reliable hermetic closure. The packaging in a carton of 9 boxes of 200 pouches meets the needs of facilities with a high volume of activity, guaranteeing constant availability of the consumable. The usual dual-material design of this type of device allows for immediate visualization of the content through the transparent face.

What are the contraindications for the use of this device?

There are no direct medical contraindications for this type of consumable, but technical usage restrictions apply. These pouches must not be used for dry heat sterilization (poupinel) if the materials are not specifically intended for this purpose, as this could lead to the degradation of the pouch or the adhesive. They must not be reused: a pouch is strictly for single use. Any perforation, tear, or significant fold before sterilization compromises the integrity of the sterile barrier. It is also advisable not to overload the pouch to avoid any rupture during the pressure increase in the autoclave.

What are the precautions for use and storage?

To guarantee the effectiveness of the sterilization pouch, the practitioner must ensure that the inserted instrument is previously cleaned, disinfected, and perfectly dried. Residual moisture can alter the quality of sterilization or damage the paper. When closing, it is crucial to smooth the self-adhesive strip well to avoid air micro-channels. After the cycle, the pouches must be stored in a dry place, away from direct light and temperature variations. The brand MEDI STOCK recommends checking the integrity of the pouch and the change of the color indicators before each clinical use to confirm that the process has been completed.

Who is the manufacturer and what standards are respected?

The product is manufactured by the manufacturer and distributed under the brand MEDI STOCK. This device is designed to meet the safety and performance requirements for the packaging of medical devices in a surgical environment. Although specific details of the CE marking or the regulatory class are not mentioned in the current technical sheet, this type of product generally follows rigorous manufacturing protocols for sterile barrier devices. Users are invited to refer to the instructions provided on the packaging and consult the manufacturer's technical notice for precise certifications and sterilization parameters compatible with reference E5017.

State of the art

Single-use sterile surgical kits significantly reduce intraoperative contamination.