20x Film Transparent Motor 40x50cm - Omnia - Delynov
The x20 film transparent moteur 40x50cm - Omnia is a medical device manufactured by Omnia S.p.A. — Class I, CE marking CE2565.
- Compliance: Medical device Class I, CE marking CE2565.
- Manufacturer: Omnia S.p.A..
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the x20 Omnia 40x50cm transparent motor film?
The x20 40x50cm transparent motor film produced by Omnia is a sterile consumable designed for the protection of motorized equipment in the operating room. This device comes in the form of a large sterile protective cover, specifically adapted to cover consoles and motors used in surgery. Its transparency is a major asset, allowing the practitioner and their assistant to maintain perfect visibility of the displayed parameters and the control interfaces of the implantology motor. As a physical barrier, it actively participates in maintaining a sterile environment around the patient, thus avoiding the risk of cross-contamination from non-autoclavable surfaces.
What are the clinical indications for this protective film?
This sterile transparent film is primarily indicated during oral surgery, implantology, and periodontology procedures requiring the use of a surgical motor. Its use is recommended whenever the motor must be placed in the immediate vicinity of the surgical field. By covering the control unit, this device transforms the equipment into a secure zone, allowing manipulation without compromising asepsis. It is particularly useful during implant placement, sinus lifts, or complex extractions where sterility management is critical. This Omnia product meets the requirements of rigorous surgical protocols in dental practices or hospital settings.
What are the technical characteristics of this device?
The surgical motor protective film from the Omnia brand features precise technical specifications to meet the needs of surgeons. Each unit has a length of 50cm and a width of 40cm, offering a generous protective surface for the majority of motors available on the market. The transparent material used is selected for its resistance and its ability not to hinder the reading of LED or LCD screens. This product is delivered in packaging of 20 units, ensuring constant availability for high-activity operating blocks. It is a Class I medical device, validated for single professional use to ensure maximum safety for each intervention.
What are the contraindications for the use of this Omnia product?
According to the data provided by the manufacturer Omnia S.p.A., there are no specific medical contraindications listed for the use of this transparent motor film. However, as with any sterile device, its use is strictly reserved for qualified healthcare professionals. The product should not be used if the individual packaging is damaged or opened before the intervention, as sterility would no longer be guaranteed. Although the material is designed for protection, it must not be misused for applications not intended by the manufacturer. Practitioners must systematically refer to the attached instructions for use to verify compatibility with their specific protocols.
What are the precautions for use for this implantology motor cover?
The use of this implantology motor cover requires strict compliance with aseptic rules during its placement. It is advised to handle the film with sterile gloves and to apply it carefully onto the previously cleaned motor. Although this film is robust, contact with sharp or rotating instruments that could puncture the protective barrier must be avoided. This product is for single use; it must under no circumstances be cleaned, disinfected, or resterilized for subsequent use. After the surgical intervention, the film must be disposed of in accordance with the infectious clinical waste (DASRI) management protocols in force at the healthcare facility.
Who is the manufacturer and what standards are respected?
This medical device is manufactured by Omnia S.p.A., a recognized manufacturer in the field of sterile solutions for dental surgery, located in Fidenza, Italy. The product complies with European legislation on medical devices, classified as Class I. It bears the CE2565 marking, certifying its compliance with the safety and performance requirements in force. Traceability and manufacturing quality are ensured by Omnia S.R.L., guaranteeing dental surgeons and implantologists reliable equipment for their operating rooms. Professionals are invited to read the instructions carefully before any use to ensure compliance with clinical standards.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
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