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Micro Cooley Tissue Forceps SinusL Handle 18cm Curved Mod - Hu-Friedy - Delynov

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The Pince à tissus Micro Cooley manche SinusL 18cm courbée mod - 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.

469.95 € 469.95 EUR 469.95 € Tax Included 700.65 €

469.95 € Tax Included 700.65 €

(0.00 € / Units)
  • Manufacturer

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Instrument

What is the Micro Cooley tissue forceps SinusL handle 18cm?

The Micro Cooley tissue forceps from the brand Hu-Friedy is a specialized microsurgery instrument for the manipulation of soft tissues. This device is distinguished by its SinusL handle and its curved configuration, offering ergonomics adapted to restricted access areas. With a length of 18cm, it allows for precise intervention in deep cavities. Manufactured by Hu-Friedy Mfg. Co., LLC, this tissue surgery forceps meets the requirements of practitioners performing complex oral surgery procedures, where the delicacy of the grip is essential to preserve the integrity of the manipulated anatomical structures.

What are the clinical indications for these curved micro forceps?

These curved micro forceps are primarily indicated for oral surgery, implantology, and periodontology procedures. They are particularly useful during guided bone regeneration (GBR) and sinus lift procedures, where the manipulation of membranes and flaps requires great finesse. The Cooley surgery forceps allows for grasping tissues without exerting excessive trauma, thus facilitating the suturing and positioning of soft tissues. Its use is strictly reserved for qualified healthcare professionals, in accordance with the recommendations of the manufacturer Hu-Friedy.

What are the technical characteristics of this instrument?

Technically, this Hu-Friedy instrument has a total length of 18cm, which classifies it among the long instruments suitable for sinus or posterior approaches. The curved Cooley forceps is equipped with specific jaws allowing for a secure grip on fine tissues. The design of the SinusL handle is studied to offer optimal balance in the hand, reducing fatigue during prolonged interventions. As a Class I device, it complies with the rigorous manufacturing standards of Hu-Friedy Mfg. Co., LLC, guaranteeing constant reliability during its use in the operating room or dental office.

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 reserved exclusively for healthcare professionals. There are no specific medical contraindications listed in the raw technical documentation, apart from general principles of surgical safety. It is imperative to read the instructions carefully before use to ensure the proper match between the instrument and the planned procedure. The practitioner must evaluate the patient's clinical status and ensure that the use of micro tissue forceps is appropriate for the morphology and pathology being treated.

What are the maintenance and durability precautions?

Although composition details are not specified, this Class I Hu-Friedy instrument must be maintained according to standard sterilization and cleaning protocols in force for reusable surgical instrumentation. To maintain the performance of the curved Cooley forceps, it is advised to follow the cleaning instructions from the manufacturer located in Chicago. Regular inspection of the jaws and the joint is necessary to guarantee a precise grip. Compliance with decontamination cycles ensures the longevity of the instrument and patient safety during oral surgery procedures.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Hu-Friedy Mfg. Co., LLC, based at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is listed under Class I according to medical device regulations. Hu-Friedy is a recognized manufacturer in the dental sector for the quality of its surgical instruments. As a Class I device, it is designed to meet safety and performance requirements for professional use. Practitioners must systematically refer to the labeling and the accompanying instructions to confirm the terms of use and specific product warnings.


State of the art

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

Specifications

Manufacturer Hu-Friedy
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