ZEPF-BIONIK BOUCHON D'IDENTIFICATION. - Helmut Zepf
The ZEPF-BIONIK BOUCHON D'IDENTIFICATION. - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 26.195.03.
- Reserved for healthcare professionals. Read instructions carefully before use.
| Manufacturer: Helmut Zepf |
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What is the ZEPF-BIONIK BOUCHON D'IDENTIFICATION?
The ZEPF-BIONIK BOUCHON D'IDENTIFICATION is an instrumental management accessory designed by Helmut Zepf Medizintechnik GmbH. This device, identified under technical reference 26.195.03, is intended to be attached to the handles or specific parts of surgical instruments. Its primary function is to allow rapid visual differentiation through color coding. Although exact composition data is not specified, this type of autoclavable silicone plug is standardized to withstand repeated sterilization cycles in oral surgery or implantology practices. It belongs to the category of technical consumables that optimize workflow within the operating block or sterilization room.
What are the clinical indications?
The use of this identification plug is indicated in all oral, periodontal, and implant surgery procedures requiring a methodical organization of instrumentation. In clinical practice, it allows for the sectorization of surgical kits by type of intervention or by practitioner within a multidisciplinary practice. This system prevents handling errors and accelerates tool recognition during critical phases of the surgical act. The color identification plug is particularly useful for marking rotary instruments, tweezers, or mirror handles, thus ensuring constant visual traceability from unpacking to the reprocessing of medical devices.
What are the technical characteristics?
The model referenced 26.195.03 by Helmut Zepf features characteristics adapted to the constraints of the surgical environment. Its design is intended to provide a stable hold on the instrument without interfering with the practitioner's grip or ergonomics. As an autoclavable silicone plug, it is developed to withstand the high temperatures and pressures encountered during steam sterilization cycles, ensuring longevity consistent with the requirements for reusable devices. Its size and shape are optimized to fit the standards of the brand's Bionik range, while remaining compatible with many diagnostic or conventional surgical instruments.
What are the contraindications for use?
Aucune contre-indication médicale spécifique n'est rapportée pour l'usage externe de ce repère d'identification sur l'instrumentation. Il est cependant essentiel de s'assurer de l'intégrité du dispositif avant chaque utilisation. Un repère présentant des signes de dégradation, tels que des fissures ou une perte d'élasticité, doit être remplacé pour éviter tout risque de détachement accidentel durant une intervention. Il est également recommandé de vérifier que le positionnement du repère n'obstrue pas les mécanismes de verrouillage ou les parties actives des instruments chirurgicaux. L'utilisation doit rester limitée à l'identification externe et ne doit en aucun cas entrer en contact prolongé avec les tissus profonds ou les muqueuses lésées.
What are the maintenance precautions?
To maintain the properties of the ZEPF-BIONIK BOUCHON D'IDENTIFICATION, it is essential to follow the cleaning and disinfection protocols recommended by Helmut Zepf Medizintechnik GmbH. This component must be cleaned at the same time as the instrument to which it is attached, using detergent and disinfectant solutions compatible with polymer or silicone materials. During autoclave sterilization, care must be taken to ensure that temperature parameters do not exceed the standard limits recommended for silicone accessories. Careful rinsing is necessary to remove any chemical residue that could alter the color or flexibility of the plug in the long term.
Who is the manufacturer and what standards are respected?
Le fabricant officiel de cet instrument est Helmut Zepf Medizintechnik GmbH, un acteur reconnu dans la fabrication d'instruments de précision pour la chirurgie orale. Concernant les normes et certifications, la classe réglementaire et le marquage CE ne sont pas explicitement spécifiés dans les données techniques disponibles pour cette référence 26.195.03. Les praticiens sont invités à se référer à la notice d'utilisation et à la documentation technique fournies par Helmut Zepf pour confirmer la conformité du produit aux exigences locales et internationales en vigueur. En tant que produit distribué par Delynov, ce bouchon répond aux standards de qualité attendus pour les accessoires de gestion d'instrumentation dans un environnement médical professionnel.
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