Bracket positioner for FIG 2 .018" system, 4 and 4.5 mm intermolar distances - Helmut Zepf (33.261.02) - Delynov
The Positionneur de bracket pour système FIG 2 .018", distances intermolaires 4 et 4,5 mm - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 33.261.02.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf FIG 2 .018" bracket positioner?
The FIG 2 .018" bracket positioner is a precision instrument designed by Helmut Zepf Medizintechnik GmbH for orthodontics. This device, referenced under code 33.261.02, is specifically structured to handle and align attachments on posterior and anterior teeth in compliance with FIG 2 technique standards. Its design is adapted for systems using .018 inch slots. This tool is distinguished by its double-ended design allowing for the measurement and stabilization of the bracket before final bonding, thus guaranteeing the reproducibility of clinical measurements essential for the success of orthodontic treatment.
What are the clinical indications for this molar bracket positioner?
This molar bracket positioner is indicated during the indirect or direct bonding phases in fixed orthodontics. It is used by the dental surgeon or orthodontist to accurately determine the placement height of brackets on molars and premolars. The use of this Helmut Zepf instrument is particularly relevant when a rigorous calibration of 4 mm or 4.5 mm is required by the treatment plan. By ensuring optimal alignment relative to the occlusal or incisal edge, it minimizes positioning errors that could lead to undesirable tooth movements or prolonged corrections at the end of treatment.
What are the technical characteristics of model 33.261.02?
The model 33.261.02 from Helmut Zepf presents strict technical specifications to meet practitioner requirements. It is calibrated for .018" bracket systems. Its FIG 2 morphology integrates two distinct measuring gauges fixed at the ends, corresponding to intermolar distances of 4 mm and 4.5 mm. This FIG 2 bracket gauge allows for direct reading and stable support on dental surfaces. The manufacturing quality of Helmut Zepf Medizintechnik GmbH ensures resistance to standard sterilization cycles in the dental office, although specific material details are not provided in the current technical sheet.
What are the contraindications for the use of this instrument?
There are no specific absolute medical contraindications for the use of a bracket positioner, other than those related to general orthodontic procedures. However, the use of this instrument is contraindicated if the dimensions of the brackets or the slot do not correspond to the specified .018" calibre, which could distort height measurements. Furthermore, its use must be avoided if the instrument shows signs of deformation or wear on the measuring gauges, as this would compromise the precision of clinical positioning. The practitioner must always verify the integrity of the tool before any intraoral intervention.
What are the maintenance precautions for this non-resorbable device?
As a manual metal instrument intended for repeated use, this bracket positioner must undergo a rigorous decontamination and sterilization protocol after each patient. Although the specific alloy details are not provided, Helmut Zepf instruments are designed to withstand conventional autoclave processes. It is recommended to carefully clean the measuring ends to remove any residue of bonding composite or dental plaque before sterilization. Regular visual inspection of the 4 mm and 4.5 mm graduations is necessary to guarantee the constant reliability of positioning during banding sessions.
Who is the manufacturer and what standards are met?
The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, a recognized player in the production of high-precision dental and surgical instrumentation. Regarding standards and certifications, the regulatory class and specific CE marking are not explicitly mentioned in the technical data provided for this reference 33.261.02. It is the responsibility of the healthcare professional to refer to the instructions for use and the markings present on the original packaging to confirm compliance with the requirements of the European Medical Device Regulation (MDR) before any clinical implementation.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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