Malo Periosteal Elevator #6 handle

What is the malo periosteal elevator handle #6?

The malo periosteal elevator handle #6 is a surgical instrumentation instrument from the brand Hu-Friedy, specifically developed for oral and implant surgery. This device belongs to the INSTRU category and is distinguished by its ergonomic configuration with a number 6 handle, offering a grip adapted to the requirements of operating theaters. As a Class I medical device, it meets the rigorous manufacturing standards imposed by the manufacturer Hu-friedy. This instrument is used to gently separate the periosteum from the bone, thus allowing effective retraction of soft tissues without compromising the integrity of adjacent structures during the preparation phases of the surgical site.

What are the clinical indications?

Clinical indications for the use of the Hu-Friedy brand malo periosteal elevator primarily include the reflection of the full-thickness flap in oral surgery. It is recommended during the placement of implants, the performance of bone grafts, or complex periodontal surgeries. Its role is crucial for detaching the mucoperiosteal flap after the incision, thus offering direct visibility on the alveolar ridge. This device is exclusively reserved for qualified healthcare professionals, such as dental surgeons and stomatologists, who master tissue manipulation techniques. The intended use by the manufacturer Hu-friedy guarantees a secure application within the framework of standardized oral surgery protocols.

What are the technical characteristics?

The malo periosteal elevator is technically characterized by its handle #6, designed to optimize control during detachment maneuvers. Manufactured under the supervision of the manufacturer Hu-friedy, this instrument from the brand Hu-Friedy is classified as a Class I medical device. Its design is focused on the robustness necessary for repeated interventions in a clinical environment. Although specific material details are not provided, its regulatory classification and industrial origin testify to compliance with professional instrumentation requirements. The geometry of the active end is specifically studied to insert under the periosteum, thus facilitating a fluid and controlled elevation of soft tissues during surgical interventions.

What are the contraindications for use?

According to information provided by the manufacturer Hu-friedy, specific contraindications are not listed exhaustively beyond general usage warnings. However, the use of the malo periosteal elevator is strictly reserved for trained healthcare professionals. An implicit contraindication lies in the use of the instrument by unqualified personnel or for procedures not intended by its initial surgical destination. It is imperative to read the instructions carefully before any use to ensure the absence of specific risks related to the patient's clinical condition or non-compliant sterilization protocols. Compliance with the indications and contraindications mentioned by the manufacturer is essential to maintain patient safety.

What are the maintenance and handling precautions?

As a non-resorbable instrument in the INSTRU category, the malo periosteal elevator requires rigorous management in terms of cleaning and sterilization between each patient. As a Class I device, it must be handled with care to preserve the integrity of its active ends. Precautions include regular inspection of the surface condition and the handle #6 to detect any sign of wear or degradation. The manufacturer Hu-friedy emphasizes that this product is reserved for healthcare professionals, which implies an in-depth knowledge of hospital or dental office decontamination cycles. Inadequate handling could alter the performance of the instrument during mucoperiosteal detachment.

Who is the manufacturer and what standards are respected?

The official manufacturer of this medical device is Hu-friedy, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. The malo periosteal elevator is marketed under the brand Hu-Friedy and complies with regulations relating to Class I medical devices. This classification guarantees that the instrument meets the essential safety and performance requirements for low-risk devices. Although CE marking is not specified in the source data, compliance with the manufacturer Hu-friedy's standards ensures industrial manufacturing quality and traceability. Practitioners are reminded that the use of this instrument must be in strict compliance with the instructions provided by the manufacturer.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.