A box of 200 self-adhesive sterilization pouches, dimensions 90 x 165 mm, self-adhesive pouch E5016 - Medi Stock (E5016) - Delynov.

What is the E5016 - Medi Stock self-adhesive pouch?

The E5016 self-adhesive pouch from the MEDI STOCK Medi Stock is a packaging device specifically designed for sterilization processes in medical and surgical environments. This sterilization envelope comes in the form of a hybrid pouch composed of a paper side and a transparent plastic film side, allowing immediate visualization of the contents. Its structure is adapted to withstand the thermal and pressure constraints encountered during steam sterilization cycles. The box contains 200 units, offering a ready-to-use solution for oral surgery practices. The MEDI STOCK offers here a compact format of 90 x 165 mm, ideal for packaging small rotary instruments, forceps, or examination mirrors.

What are the clinical indications for this packaging?

In clinical practice, the dental self-adhesive pouch is indicated for the protection of surgical instrumentation after the decontamination cycle. It is used systematically before going into the autoclave to ensure that the instruments remain isolated from any environmental contamination until their use at the chairside. This type of self-adhesive sterilization pouch is perfectly suited for implantology, muco-gingival surgery, or complex extractions. The use of this 90x165 sterilization pouch allows for the organization of surgical kits by procedure, thus facilitating stock management and compliance with the rigorous hygiene protocols imposed in modern dental care facilities.

What are the technical characteristics of reference E5016?

The technical reference E5016 corresponds to a self-adhesive autoclave pouch with precise dimensions of 90 x 165 mm. Its main characteristic lies in its integrated closure system: a pre-applied adhesive strip that allows the pouch to be hermetically sealed without requiring the use of a heat sealer. This technical specificity ensures significant time savings during the packaging phase. The material used by the manufacturer allows effective penetration of the sterilizing agent while constituting a robust microbiological barrier after drying. The transparency of the upper film facilitates rapid identification of the packaged medical devices, thus reducing unnecessary handling before the operative procedure.

What are the contraindications for the use of these pouches?

Although the source data does not specify direct medical contraindications, the use of this sterilization packaging must respect the technical limits of the product. It must not be used with sterilization methods that are incompatible with paper or plastic film, such as dry heat (poupinel), which could deteriorate the materials and compromise the seal. It is also contraindicated to use a pouch showing a tear, perforation, or sealing defect, as the integrity of the sterile barrier would no longer be guaranteed. Overloading the pouch should be avoided to prevent any rupture of the film or paper during the pressure increase in the autoclave.

What are the precautions for use to maintain sterility?

To guarantee the effectiveness of the self-adhesive sterilization pouch, several precautions must be observed by the assistant or practitioner. When pouching, it is crucial not to trap too much air before closing the adhesive strip to avoid bursting during the cycle. After sterilization, the pouches must be stored in a dry place, away from light and temperature variations. Any trace of moisture on the paper after the cycle indicates a drying defect that compromises sterility. The MEDI STOCK recommends checking the integrity of the seal before each opening. Opening must be done aseptically, by peeling the two sides without touching the internal instrument.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is identified as the manufacturer, distributed under the MEDI STOCK Medi Stock. Regarding standards and regulatory classification, the data provided does not specify a medical device class or any particular CE marking for this reference E5016. However, this type of consumable is generally designed to meet the requirements of dental and hospital practice regarding the packaging of medical devices. For any precise information concerning ISO certifications or compliance with European sterilization standards, it is imperative to refer to the product labeling or the technical documentation provided by the manufacturer accompanying the box of 200 units.

State of the art

Surgical medical consumables play a decisive role in operative safety.