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Hemostatic forceps Halsted-Mosquito no.3 12cm curved - Hu-Friedy - Delynov

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The Pince hémostatique Halsted-Mosquito #3 12cm courbée - 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.

44.40 € 44.4 EUR 44.40 € Tax Included

44.40 € Tax Included

(0.00 € / Units)
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Instrument

What is the Hu-Friedy Halsted-Mosquito #3 hemostatic forceps?

The Halsted-Mosquito #3 hemostatic forceps is a precision instrument manufactured by Hu-Friedy Mfg. Co., LLC. This device is characterized by a fine metallic structure with a curved working part, specifically designed for surgical procedures requiring great finesse. Its 12cm length makes it a compact tool, ideal for navigating the oral cavity during oral surgery interventions. As an instrument in the GBR category, these halsted surgery forceps meet the quality requirements of the manufacturer Hu-Friedy, recognized for its expertise in high-performance dental and surgical instrumentation.

What are the clinical indications for this instrument?

In clinical practice, the halsted hemostatic forceps are primarily indicated for hemostasis, allowing for the temporary clamping of small-caliber vessels to interrupt blood flow. It is particularly useful during periodontal surgeries, pre-implant surgeries, or guided bone regeneration (GBR) procedures. Beyond its primary function, practitioners frequently use it for the precise manipulation of flaps, the removal of small tissue fragments, or grasping suture materials. Its curvature allows for reaching posterior areas or deep surgical sites with optimal visibility.

What are the technical characteristics of the 12cm hemostatic forceps?

The Hu-Friedy 12cm hemostatic forceps feature strict technical characteristics to meet the needs of dental surgeons. It has a total length of 12 cm, which classifies it among the 'Mosquito' models, smaller than standard Halsted forceps. The active part is curved, facilitating passage behind anatomical structures or into interproximal spaces. The ratchet locking mechanism allows for maintaining constant pressure without continuous manual effort, thus ensuring safety during vascular clamping or prolonged tissue holding.

What are the contraindications for the use of this device?

According to the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is strictly reserved for qualified healthcare professionals. There are no specific medical contraindications listed in the raw technical documentation, other than the standard precautions related to sterility and the integrity of the instrument. It is imperative not to use the forceps on structures for which they are not dimensioned, such as large-caliber vessels requiring more robust forceps, to avoid any risk of tissue trauma or instrument breakage.

What are the maintenance and durability precautions?

Although this product is non-resorbable, its durability depends on compliance with cleaning and sterilization protocols. Like any Class I surgical instrument, it must be inspected before each use to check the alignment of the jaws and the effectiveness of the locking system. The halsted surgery forceps must be cleaned with pH-neutral solutions to avoid corrosion. It is recommended to carefully follow the instructions for use provided by Hu-Friedy to guarantee the longevity of the instrument and maintain its mechanical properties during repeated autoclave cycles.

Who is the manufacturer and what standards are respected?

These forceps are manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. From a regulatory standpoint, this medical device is classified as Class I. The manufacturer Hu-Friedy is globally recognized for respecting rigorous manufacturing standards. Although specific CE marking is not detailed in the source data, the product complies with the regulatory requirements applicable to medical devices of this class. Professionals must read the instructions carefully before any use to ensure compliance with safety recommendations.


State of the art

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

Specifications

Manufacturer Hu-Friedy
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