CARBIDE BURS-FGL-HM207- Meisinger - Hager & Meisinger GmbH (2300207315010) - Delynov
The FRAISES CARBURE-FGL-HM207- Meisinger - Hager & Meisinger GmbH is a medical device manufactured by Hager & Meisinger GmbH — Class IIa, CE marking CE0044.
- Compliance: Medical device Class IIa, CE marking CE0044.
- Manufacturer: Hager & Meisinger GmbH.
- Reference: 2300207315010.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Meisinger FGL-HM207 bur?
The Meisinger FGL-HM207 bur is a high-precision rotary instrument manufactured by Hager & Meisinger GmbH. It is a carbide FGL (Friction Grip Long) bur primarily used in oral and maxillofacial surgery. Its tungsten carbide structure provides optimal hardness for working on mineralized tissues. This device is identified under reference 2300207315010 and belongs to the category of surgical consumables for dental offices and hospitals. As a specialized rotary instrument, it is designed to fit handpieces compatible with the FGL standard, offering a reliable solution for bone cutting and milling procedures.
What are the clinical indications for this surgical carbide bur?
This FGL dental bur is indicated for a wide range of procedures in dentistry, implantology, bone treatment, and maxillary surgery. It is particularly sought after during preoperative planning and technical execution phases requiring precise removal of bone material or sectioning of complex dental elements. Its use is strictly reserved for qualified practitioners, such as dental surgeons or doctors with advanced training in dental implantology. The choice to use this surgical carbide bur rests on the practitioner's decision, evaluating the clinical situation and the patient's specific indication on a case-by-case basis to ensure the safety of the operative procedure.
What are the technical characteristics of the product?
The Meisinger HM207 bur is distinguished by its carbide composition, a material recognized for its superior resistance during intense mechanical stress. This model adopts the FGL shank standard, facilitating its integration into rotary surgical equipment. The manufacturer, Hager & Meisinger GmbH, ensures manufacturing complies with the strict requirements of the medical sector. The device is regulatory classified as Class IIa, attesting to its compliance with safety standards for invasive devices for surgical use. Each unit is associated with reference code 2300207315010, guaranteeing precise traceability within the clinical inventory and during chairside use.
What are the contraindications for the use of this instrument?
The use of the Meisinger FG or FGL carbide bur is contraindicated for any practitioner who does not have the required knowledge or solid experience in maxillary surgery or implantology. Use that does not comply with the manufacturer's specifications can lead to premature wear of the device and involve direct risks for patients as well as users. Although specific medical contraindications are not exhaustively listed in the raw documentation, it is up to the doctor to decide, under their sole responsibility, the suitability of the instrument based on the patient's health status and the complexity of the planned intervention.
What are the precautions for use and maintenance?
The use of Meisinger surgical devices assumes technical know-how and adequate experience in the fields of diagnosis and operative techniques. To prevent any incident, the practitioner must systematically refer to the manufacturer's specifications available in the official catalog. It is crucial to note that any non-compliant use can compromise the integrity of the FGL carbide bur. In the event of a serious incident occurring in connection with the device, immediate notification must be made to the manufacturer Hager & Meisinger GmbH as well as to the competent authority of the Member State concerned. Regular continuing education is recommended to master the possible applications and safety protocols related to these rotary instruments.
Who is the manufacturer and what standards are respected?
The official manufacturer of this device is Hager & Meisinger GmbH, located in Neuss, Germany. This recognized manufacturer complies with the strictest European quality standards. The product benefits from the CE0044 marking, confirming its compliance with the regulatory requirements in force for medical devices. Classified as Class IIa, this instrument meets the safety and performance criteria essential for surgical practice. Meisinger also offers continuing education sessions to support specialists in the optimal use of their devices. All technical information and possible applications are detailed by the manufacturer to ensure safe and effective use in a medical environment.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Meisinger |
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