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Stainless Steel Dam Punch - Helmut Zepf (19.010.00) - Delynov

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The Perforateur à digue en acier inoxydable - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 19.010.00.
  • Reserved for healthcare professionals. Read instructions carefully before use.

181.05 € 181.05 EUR 181.05 € Tax Included

181.05 € Tax Included

(181.05 € / Units)
  • Manufacturer

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Instrument

What is the Helmut Zepf rubber dam punch (19.010.00)?

The Helmut Zepf rubber dam punch, referenced under code 19.010.00, is a manual dental instrument designed for the preparation of the operative field. Manufactured by Helmut Zepf Medizintechnik GmbH, this device is crafted from high-quality medical stainless steel to meet the requirements of dental surgery and endodontics. This steel rubber dam punch is distinguished by its robust structure and its ability to precisely perforate dam sheets before their positioning in the mouth. As a Class I medical device, it is specifically intended for professional use in dental practices to effectively isolate the working area from oral fluids and contaminants.

What are the clinical indications for this instrument?

The intended use of the Helmut Zepf punch is as a manual dental instrument for placing the rubber dam. Its primary indication is the isolation of the operative field during conservative care, endodontic treatments, or bonding procedures requiring a dry environment free of saliva. By using this rubber dam punch, the practitioner can calibrate the necessary opening for each tooth, thus ensuring optimal sealing. Helmut Zepf instrumentation is recognized for its reliability in these clinical protocols where moisture management and patient airway protection are critical.

What are the technical characteristics of the 19.010.00 punch?

The Helmut Zepf 19.010.00 punch is a hinged instrument designed in medical stainless steel, a material chosen for its resistance to repeated processing cycles. Its ergonomic design allows for easy handling to punch different hole diameters according to the needs of the dentition being treated. This device belongs to the category of consumables and reusable instruments (Class I). It is delivered non-sterile by the manufacturer Helmut Zepf Medizintechnik GmbH. Before any use, the practitioner must check for the absence of visible damage, such as cracks, breaks, or defects on the cutting edges, to guarantee patient safety and perforation efficiency.

What are the contraindications for the use of this rubber dam punch?

The main contraindication related to the use of this medical stainless steel instrument concerns hypersensitivity or intolerance to metals. If the patient has a known allergy to steel components, contact with the instrument may trigger an adverse reaction. The manufacturer states that if such a hypersensitivity reaction occurs during the procedure, the procedure must be immediately stopped and the necessary medical measures must be taken. It is therefore imperative to validate the patient's anamnesis regarding metal allergies before using this steel rubber dam punch.

What are the maintenance and reprocessing precautions?

Like any Helmut Zepf instrument, the punch must imperatively be cleaned, disinfected, and sterilized before the first use as well as after each subsequent use. The reprocessing process must be complete to guarantee asepsis. The manufacturer emphasizes that it is crucial to inspect the instrument for any visible wear before use. Due to the product design and the materials used, there is no defined maximum limit for the number of processing cycles, as long as the instrument does not show structural defects or corrosion. The use of damaged or worn products is strictly prohibited to avoid any clinical risk.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This recognized manufacturer complies with the regulatory requirements for medical devices, classifying this punch as Class I. The product is delivered non-sterile and requires a rigorous sterilization protocol under the responsibility of the healthcare professional. Traceability is ensured by the reference 19.010.00. In accordance with the manufacturer's directives, the use of this instrument is strictly reserved for qualified healthcare professionals, thus ensuring an application compliant with the safety and hygiene standards in force in the dental sector.


State of the art

Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer Helmut Zepf
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