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Miller Crown Remover - Helmut Zepf (19.273.00)

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The Arrache-couronnes Miller - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 19.273.00.
  • Reserved for healthcare professionals. Read instructions carefully before use.

110.03 € 110.03 EUR 110.03 € Tax Included

110.03 € Tax Included

(110.03 € / Units)
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Instrument

What is the Miller crown remover - Helmut Zepf (19.273.00)?

The Miller crown remover, referenced under code 19.273.00, is a manual dental instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This device is manufactured from high-quality medical stainless steel, ensuring resistance adapted to mechanical stresses during prosthetic removal procedures. As an instrument in the CONSO category at Delynov, it is part of the classic arsenal of practitioners for the management of fixed prosthetic elements. Its specific design according to the Miller model meets the grip and force transmission requirements necessary to release crowns from their support without damaging the underlying structures.

What are the clinical indications for this instrument?

The main indication for this manual instrument is the removal of prosthetic devices in the oral environment. It is used by healthcare professionals during prosthetic revision procedures, treatment of decay under crowns, or pre-implant surgeries requiring the removal of old bridges. Its use is strictly reserved for qualified healthcare professionals. The instrument allows for controlled traction to break the cement seal of the crowns. It is essential to check for the absence of visible damage, such as cracks or defects on the edges, before any clinical application to ensure patient safety.

What are the technical characteristics of the Miller crown remover?

The Miller crown remover (reference 19.273.00) is a non-sterile instrument upon delivery. Its major technical characteristic lies in its composition of medical stainless steel, a standard material for surgical instrumentation. The manufacturer, Helmut Zepf Medizintechnik GmbH, emphasizes that the product design and materials used do not allow for the definition of a maximum limit of processing cycles. However, the lifespan of the instrument depends directly on maintenance and the absence of visible wear. It must be systematically cleaned, disinfected, and sterilized before the first use and after each subsequent use to maintain its functional properties.

What are the contraindications for the use of this instrument?

The main medical contraindication mentioned by the manufacturer Helmut Zepf concerns hypersensitivity to metals. Contact with medical stainless steel can trigger an allergic reaction in patients with a known intolerance to its components. If such a hypersensitivity reaction occurs during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken. Furthermore, the use of the instrument is contraindicated if it shows visible damage, breaks, or pronounced wear, as this could compromise the safety of the operative act or injure the surrounding tissues.

What are the maintenance and reprocessing precautions?

As the instrument is delivered non-sterile, a strict cleaning, disinfection, and sterilization protocol is mandatory before the first use. This procedure must be repeated after each intervention. It is crucial to inspect the instrument for any trace of corrosion, cracks, or defects on the active parts before use. Helmut Zepf specifies that, although no limit on processing cycles is set, the use of damaged products is prohibited. Compliance with these maintenance instructions not only guarantees the longevity of the stainless steel but also prevents the risks of cross-contamination between patients in dental offices or hospital settings.

Who is the manufacturer and what standards are respected?

The Miller crown remover is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I according to current regulations. The manufacturer ensures the compliance of its instruments with safety and performance requirements for manual devices. As a Class I product, it meets the strict manufacturing standards imposed by the European Medical Device Regulation (MDR). Healthcare professionals can refer to the instructions provided by Helmut Zepf to ensure use in accordance with the intended purpose, thus guaranteeing the traceability and safety of the care provided.


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Surgical medical consumables play a decisive role in operative safety.

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Manufacturer Helmut Zepf
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