EXTRACT. FORCEPS, ENGL. PATTERN, FIG.22 FOR CHILDREN, ROBA DESIGN - Helmut Zepf (10.685.22ZD) - Delynov
The EXTRACT. FORCEPS, ENGL. PATTERN, FIG.22FOR CHILDREN, ROBA DESIGN- Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 10.685.22ZD.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf child molar forceps (10.685.22ZD)?
This device is a pediatric dental forceps specifically designed by Helmut Zepf for the extraction of primary molars. This model belongs to the ROBA Design range, characterized by beak ergonomics studied to match the morphology of temporary teeth. This forceps adopts the English Pattern configuration under the reference Fig.22, adapted for the lower quadrants. Its robust metallic structure is designed to meet the requirements of pediatric oral surgery, offering a firm grip on the crown to minimize the risk of root fracture during luxation and avulsion.
What are the clinical indications for this pediatric forceps?
The Fig.22 child molar forceps is primarily indicated for the avulsion of mandibular temporary molars. In clinical practice, it is used by dental surgeons and pedodontists to treat non-restorable caries, pulp necrosis, or to facilitate the eruption of permanent teeth in cases of orthodontic crowding. Its ROBA Design allows for precise adaptation to the neck of the primary tooth, ensuring uniform pressure distribution. This type of pediatric dental forceps is essential for oral surgery interventions in young patients where precision of movement is paramount.
What are the technical characteristics of reference 10.685.22ZD?
The 10.685.22ZD model is distinguished by its Fig.22 configuration complying with the English Pattern standard, specifically sized for the practitioner's hand and the child's oral cavity. The beaks are designed to insert effectively at the level of the furcation of the primary lower molars. The Helmut Zepf ROBA design integrates surface characteristics and handle curvature optimized to prevent slipping during rotation and tilting movements. This child molar forceps is manufactured with materials resistant to repeated autoclave sterilization cycles, guaranteeing increased longevity within the dental office.
What are the contraindications for the use of this forceps?
Contraindications for the use of this child molar forceps are mainly related to clinical situations where direct mechanical extraction is prohibited or risky. This includes cases of excessive proximity to the germs of permanent teeth without prior planning, or in the presence of uncontrolled systemic pathologies in the child (severe coagulation disorders). It must not be used on permanent teeth, as its beaks are sized exclusively for primary anatomy. Any use outside the field of tooth extraction, such as the manipulation of other devices or materials, is strictly discouraged to avoid damaging the instrument.
What are the maintenance and durability precautions?
To maintain the effectiveness of the Helmut Zepf forceps, a strict decontamination and sterilization protocol must be followed after each intervention. Although this product is not an absorbable suture, its durability depends on the quality of manual cleaning or thermal disinfection to eliminate any organic residue in the hinges. It is recommended to regularly check the alignment of the beaks and the fluidity of the joint. The use of non-corrosive cleaning solutions is imperative to preserve the integrity of the instrument. Storage in a dry and sterile environment after processing guarantees microbiological safety for subsequent oral surgery procedures.
Who is the manufacturer and what standards are respected?
The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, a company recognized in the dental surgical instrumentation sector for its German manufacturing quality. The product is marketed under the Helmut Zepf brand, a guarantee of technical precision. Regarding specific standards and certifications such as the regulatory class or CE marking, this information is not specified in the current technical documentation. It is the practitioner's responsibility to consult the instructions for use provided by the manufacturer and to comply with current local directives regarding the use of reusable medical devices in a surgical environment.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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