New Set Chiropro Plus including 1 20:1L Contra-angle + 50 irrigation lines - Bienair (1700709-001)

What is the New Chiropro Plus 3rd Gen Set?

The New Chiropro Plus 3rd Gen Set, referenced under code 1700891-001 by the brand Bien-Air Medical Technologies, is a complete system designed for specialized surgical interventions. This dental surgery motor integrates a third-generation control console, a 20:1L Micro-Series contra-angle with light, as well as a wireless pedal for fluid parameter management. This device is specifically configured to meet the requirements of modern implantology. The set is delivered with 50 irrigation lines, guaranteeing optimal tissue cooling during drilling phases. It is a robust professional equipment developed by the manufacturer Bien-Air Dental SA, recognized for its reliability in the field of rotary instrumentation.

What are the clinical indications for this implantology motor?

This implantology motor with contra-angle is indicated for a wide spectrum of oral surgery procedures. According to the manufacturer's data, the device is primarily intended for dental implantology, including the preparation of the implant bed and the insertion of implants. It also finds application in periodontology for surgical treatments of supporting tissues, as well as in oral surgery and maxillofacial surgery for bone resection or remodeling acts. The use of this Bien-Air Medical Technologies equipment is strictly reserved for qualified healthcare professionals, ensuring implementation in accordance with clinical protocols in force in dental offices and hospital centers.

What are the technical characteristics of the Chiropro Plus set?

The Chiropro Plus 3rd Gen set is distinguished by the inclusion of the 20:1L Micro-Series contra-angle, which optimizes balance in hand and access to posterior areas. This surgical implantology motor is controlled by a wireless pedal, eliminating floor clutter and facilitating chairside ergonomics. Reference 1700891-001 also includes 50 sterile irrigation lines, essential for preventing thermal heating of the alveolar bone. Torque and speed management is configurable via an intuitive interface, allowing precise adaptation to the different bone densities encountered in implantology. The Micro-Series technology from the brand Bien-Air Medical Technologies ensures stable power transmission for increased operational safety.

What are the contraindications for the use of this device?

The manufacturer Bien-Air Dental SA does not list specific medical contraindications related to materials in the documentation provided; however, the use of this dental surgery motor is conditioned by the patient's general state of health and the classic contraindications related to oral or maxillofacial surgery. It is imperative to read the instructions for use carefully before any intervention. Like any Class IIa electromedical device, its use must be evaluated by the practitioner based on the benefit/risk ratio for the patient, particularly in the presence of implanted electronic devices or serious systemic pathologies that could interfere with the planned surgical act.

What are the precautions for use and maintenance?

The use of the Chiropro Plus 3rd Gen requires strict compliance with asepsis protocols. The provided irrigation lines are for single use to prevent any risk of cross-contamination. The Micro-Series implantology contra-angle must be maintained according to the manufacturer's precise recommendations to maintain its mechanical performance and longevity. It is essential to check the integrity of the wireless pedal and the console before each intervention. As the device is reserved for healthcare professionals, prior training on the Bien-Air Medical Technologies brand control system is advised to fully exploit the safety features, such as torque control during the final phase of implant placement.

Who is the manufacturer and what standards are met?

The Chiropro Plus 3rd Gen set is manufactured by Bien-Air Dental SA, located at Länggasse 60, CH-2504 Bienne, Switzerland. This medical device belongs to Class IIa and bears the CE0123 marking, certifying its compliance with European regulatory requirements relating to medical devices. Traceability is ensured by product reference 1700891-001. As a recognized manufacturer, Bien-Air Dental SA guarantees that this system meets the safety and performance standards necessary for the practice of implantology, periodontology, and maxillofacial surgery. Practitioners must systematically refer to the technical notice to ensure use in accordance with the Bien-Air Medical Technologies brand directives.

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