Needle holder Lichtenberg PermaSharp 20cm - Hu-Friedy - Delynov

What is the Lichtenberg PermaSharp 20cm needle holder?

The Lichtenberg PermaSharp 20cm needle holder is a manual surgical instrument developed by Hu-Friedy, a recognized manufacturer in the field of odontological instrumentation. This device is specifically designed for grasping and firmly holding suture needles during surgical procedures. Its elongated 20cm structure allows access to posterior or deep areas of the oral cavity with optimal visibility. As a product of the PermaSharp range, it meets the quality requirements of practitioners performing oral and implant surgery. This device belongs to Class I of medical devices, guaranteeing its compliance with regulatory standards for non-invasive or reusable instruments after sterilization.

What are the clinical indications for this Hu-Friedy instrument?

The Hu-Friedy lichtenberg needle holder is indicated for all oral surgery procedures requiring flap closure or graft stabilization by suture. It is particularly used in implantology for sutures after implant placement, in periodontology for muco-gingival surgeries, as well as in general oral surgery for complex extractions or apical resections. Its 20cm length is a major clinical asset for working in difficult-to-access sectors without obstructing the operative field. This device is exclusively reserved for use by qualified healthcare professionals, trained in surgical suture techniques, in accordance with the directives of the manufacturer Hu-Friedy Mfg. Co., LLC.

What are the technical characteristics of the Lichtenberg needle holder?

Technically, this needle holder is distinguished by a total length of 20cm, offering leverage and reach adapted to extensive oral surgery interventions. Hu-Friedy's PermaSharp technology ensures a reliable gripping interface between the instrument and the suture needle, reducing the risk of slipping or unintended rotation during passage through tissues. The locking mechanism is designed to maintain constant pressure without damaging the needle body. Although the exact composition is not specified in the source data, manufacturing by Hu-Friedy guarantees an instrument meeting Class I requirements, intended to be sterilized and reused according to hospital and dental office decontamination protocols.

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 needle holder is strictly reserved for healthcare professionals. There are no specific medical contraindications listed other than those related to standard surgical protocols. However, the instrument must not be used for applications other than those intended, such as handling non-surgical materials or heavy metal wires that could damage the jaws. Practitioners should refer to the instructions for use to check for any contraindications related to the patient's health status or specific sensitivities, although the raw MDR text does not mention any particular allergy or intolerance for this Class I instrument.

What are the maintenance and durability precautions?

As a non-resorbable and reusable instrument, the 20cm Lichtenberg needle holder requires a rigorous sterilization protocol between each patient. The manufacturer Hu-Friedy emphasizes the importance of reading the instructions carefully before use to ensure the longevity of the instrument and the safety of care. It is recommended to check the integrity of the jaws and the closing mechanism before each intervention. Proper cleaning to remove biological debris is essential before autoclaving. Compliance with the sterilization cycles recommended by Hu-Friedy maintains the performance of the PermaSharp range, thus ensuring precise handling of needles over the long term without alteration of the clamping quality.

Who is the manufacturer and what standards are respected?

The Lichtenberg PermaSharp needle holder is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This manufacturer is globally recognized for the quality of its surgical instruments. This product is classified as a Class I medical device, which implies that it meets the essential safety and performance requirements defined by the regulations in force for this category of instruments. Although specific CE marking is not mentioned in the source data, the Class I status and the Hu-Friedy manufacturing origin guarantee strict quality control. Healthcare professionals must consult the enclosed instructions to ensure compliance with the warnings and conditions of use provided by the manufacturer.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.