Prichard PPR3 Periosteal Elevator - Helmut Zepf (41.878.14) - Delynov

What is the Helmut Zepf Prichard PPR3 periosteal elevator?

The Prichard PPR3 periosteal elevator, referenced under code 41.878.14 at Delynov, is a high-precision manual dental instrument manufactured by Helmut Zepf Medizintechnik GmbH. Made of medical stainless steel, this instrument is specifically structured to meet the requirements of oral surgery. Its material composition ensures the necessary resistance to repeated sterilization cycles while guaranteeing standard biocompatibility for oral tissues. As a Class I device, it is part of the arsenal of non-invasive surgical instruments intended for soft tissue manipulation.

What are the clinical indications for this instrument?

The Prichard PPR3 periosteal elevator is indicated for dental and oral surgery procedures requiring the reflection of a full-thickness flap. Its primary use lies in the elevation of the periosteum from the alveolar bone, thus exposing the surgical field during implant placement, periodontal surgery, or apical resections. The instrument allows the practitioner to maintain adequate visibility by retracting soft tissues in a stable manner. Its use is strictly reserved for qualified healthcare professionals mastering oral surgery techniques.

What are the technical characteristics of the 41.878.14 elevator?

This medical device, identified by reference 41.878.14, is manufactured by Helmut Zepf from high-quality medical stainless steel. It belongs to the category of Class I manual instruments according to current regulations. The product is delivered non-sterile and requires a complete reprocessing protocol before each use. Due to its robust design and the materials used, the manufacturer does not establish a defined maximum limit for the number of treatment cycles, although the instrument must be visually inspected for any signs of wear or damage before each intervention.

What are the contraindications for the use of this Helmut Zepf instrument?

The main contraindication related to the use of the Prichard PPR3 periosteal elevator is known hypersensitivity or intolerance to metals, particularly to the components of medical stainless steel. If a hypersensitivity reaction is triggered in the patient upon contact with the instrument, the procedure must be stopped immediately. Necessary clinical measures must then be taken accordingly. It is therefore imperative to check the patient's allergic history before any surgical intervention involving this metallic instrument.

What are the maintenance and safety precautions?

All Helmut Zepf instruments must imperatively be cleaned, disinfected, and sterilized before the first use, as well as after each subsequent use. It is crucial to perform a complete cleaning to remove all residues before sterilization. Before each use, the practitioner must inspect the instrument for visible damage such as cracks, breaks, or defects on the cutting edges. The use of damaged or worn products is strictly prohibited to guarantee patient safety and the effectiveness of the surgical procedure.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This periosteal elevator is a Class I medical device, compliant with regulatory requirements for manual dental instruments. The manufacturer emphasizes that its products are delivered non-sterile and that their compatibility with other products used during surgery must be verified beforehand. The reprocessing process is possible without a predefined cycle limit, subject to maintaining the physical integrity of the medical stainless steel.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.