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Surgical Fabric Forceps Semkin Taylor No. 34 1X2 Curved 12.5cm - Hu-Friedy - Delynov

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The Pince/tissus Semkin Taylor #34 chirurg. 1X2-courbée 12,5cm - Hu-Friedy is a medical device manufactured by Hu-Friedy Mfg. Co., LLC.

  • Compliance: Medical device Class I.
  • Manufacturer: Hu-Friedy Mfg. Co., LLC.
  • Reserved for healthcare professionals. Read instructions carefully before use.

42.15 € 42.15 EUR 42.15 €excl. VAT

42.15 €excl. VAT

(0.00 € / Units)
  • Manufacturer

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Instrument
Manufacturer: Hu-Friedy

What are the Hu-Friedy Semkin Taylor #34 surgical forceps?

The Semkin Taylor #34 surgical forceps from the brand Hu-Friedy are a precision instrument designed for micro-surgery and fine manipulation of soft tissues. This specific model features a curved tip and a 1X2 tooth configuration, meaning one tooth interlocks between two others to ensure a firm grip without excessive crushing of anatomical structures. With a length of 12.5cm, this instrument is manufactured by Hu-Friedy Mfg. Co., LLC, a recognized manufacturer in the field of surgical instrumentation. It belongs to the category of GBR (Guided Bone Regeneration) and periodontology devices, where delicacy of movement is paramount for post-operative healing.

What are the clinical indications for these curved tissue forceps?

These curved tissue forceps are primarily indicated for oral surgery interventions requiring high dexterity. They are used by dental surgeons and implantologists to grasp, lift, or stabilize mucosal flaps during incision and suturing phases. Its specific curvature is ideal for reaching posterior sectors or restricted access areas where straight forceps would be less ergonomic. It finds its application in guided bone regeneration (GBR) procedures, gingival grafts, and implant placement surgeries. The 1X2 configuration allows for tissue maintenance with controlled pressure, thus preventing slippage during the passage of the suture needle.

What are the technical characteristics of this instrument?

The Semkin Taylor #34 tissue forceps are distinguished by several precise technical characteristics. They measure 12.5cm long, a standard dimension allowing for optimal control between the practitioner's fingers. The working part is curved, offering better visibility of the surgical field. The jaws are equipped with a 1X2 tooth system, guaranteeing a secure grip on connective and epithelial tissues. Manufactured by Hu-Friedy, this instrument meets the quality requirements of the manufacturer Hu-Friedy Mfg. Co., LLC. As a Class I medical device, it is designed to be reusable after an appropriate cleaning and sterilization cycle, in accordance with the protocols in force in dental offices and oral surgery centers.

What are the contraindications for the use of this device?

According to the information provided by the manufacturer Hu-Friedy, the use of this instrument is strictly reserved for qualified healthcare professionals. There are no specific medical contraindications listed other than those related to standard surgical protocols. However, the practitioner must ensure that the instrument is used in accordance with its intended use, namely the manipulation of soft tissues. Inappropriate use on hard structures such as bone or for tightening screws could damage the 1X2 teeth and compromise the precision of the forceps. It is imperative to read the instructions carefully before use to respect the safety and maintenance instructions recommended by Hu-friedy 3232 N. Rockwell St. Chicago.

What are the maintenance precautions for these curved surgical forceps?

As a non-resorbable and reusable instrument, the Semkin Taylor curved surgical forceps require rigorous maintenance. After each intervention, they must be cleaned, decontaminated, and sterilized according to the Hu-Friedy manufacturer's instructions. It is advisable to regularly inspect the alignment of the 1X2 teeth and the condition of the hinge to ensure smooth operation. Particular attention must be paid during the cleaning of the curved jaws to eliminate any biological residue. Compliance with sterilization cycles is crucial to maintain the integrity of the Class I device and ensure patient safety during subsequent interventions. Storage in a dry and clean environment is recommended to prevent any premature corrosion of the instrumentation.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. Hu-Friedy is a historical player recognized for the quality of its manual instrumentation in dentistry. This product is classified as a Class I medical device. This classification implies that the manufacturer guarantees the instrument's compliance with essential safety and performance requirements. Although CE marking is not specifically detailed in the source data, belonging to Class I under the Medical Device Regulation (MDR) confirms its regulated status for professional use in a clinical setting. Practitioners should refer to the instructions for use for all information relating to implementation and safety standards.


State of the art

Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.

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Ordered before 2 pm, delivered within 24 h. Otherwise, within 72 h.

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