PRICHARD PERIOSTEAL ELEVATOR PPR3 - Helmut Zepf (41.878.11ZS) - Delynov

What is the PRICHARD RASPATORIUM PPR3?

The PRICHARD RASPATORIUM PPR3, bearing reference 41.878.11ZS, is a precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. This dental surgery raspatorium is designed from medical-grade stainless steel, ensuring compatibility with rigorous cleaning and sterilization protocols. As a Class I device, it features a robust structure adapted to the requirements of oral surgery. Its specific design allows the practitioner to manipulate tissues with great control, thereby facilitating access to complex surgical sites while respecting the integrity of surrounding structures.

What are the clinical indications?

This Prichard raspatorium is primarily indicated for dental and oral surgery interventions requiring action on the tooth or dental apparatus. Its intended use includes the elevation and retraction of the periosteum to expose the alveolar bone, a crucial step in periodontology, implantology, or complex extraction procedures. The Helmut Zepf instrument serves as a manual tool to delicately separate soft tissues from the bone surface, allowing for optimal visibility and a clear working field for the surgeon during surgical treatment.

What are the technical characteristics?

The Helmut Zepf device (reference 41.878.11ZS) is characterized by its manufacture in medical stainless steel, a material chosen for its resistance to thermal and chemical treatment cycles. It is a Class I instrument delivered non-sterile. Its morphology is specifically adapted for dental Prichard elevator functions, offering precise working ends for blunt dissection. Due to its design and the materials used, the manufacturer states that there is no defined maximum limit for the number of reprocessing cycles, although wear must be checked before each use.

What are the contraindications for use?

The main medical contraindication mentioned by the manufacturer Helmut Zepf concerns known intolerance or hypersensitivity to metals. Contact of medical stainless steel with the patient's tissues can trigger a hypersensitivity reaction in predisposed subjects. If such a reaction occurs during the intervention, the procedure must be immediately interrupted and the necessary clinical measures must be taken. It is therefore imperative to check the patient's allergic history before any use of this surgical 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. Before any intervention, the practitioner must visually inspect the product to detect possible damage or visible wear, such as cracks, breaks, or defects on the cutting edges. The use of damaged or worn products is strictly prohibited. Compatibility with other instruments must also be verified beforehand to ensure the safety of the surgical treatment.

Who is the manufacturer and what standards are respected?

The PRICHARD RASPATORIUM PPR3 is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I according to current regulations. It is delivered non-sterile and its maintenance is the responsibility of qualified healthcare professionals. The manufacturer emphasizes that the instrument is exclusively reserved for professional use. Compliance with reprocessing protocols (cleaning, disinfection, and sterilization) is essential to maintain the conformity and safety of the instrument during its use in dental offices or hospital environments.

State of the art

Surgical medical consumables play a decisive role in operative safety.