Bird beak forceps 0.020 fine inch - Hu-Friedy - Delynov
The Pince bec oiseau<=0.020 inch fine - 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.
What are the Hu-Friedy fine bird beak pliers?
The fine bird beak pliers, developed by the manufacturer Hu-Friedy, are a specialized manual instrument used primarily for metal wire work. Their structure is characterized by specific jaws allowing for complex bends and loops on wires with a diameter less than or equal to 0.020 inch (0.51 mm). This Class I medical device is designed to meet the requirements for finesse during interventions requiring delicate manipulation of equipment. As precision orthodontic pliers, they ensure optimal control during forming, thus guaranteeing a perfect adaptation of the devices to the patient's clinical needs.
What are the clinical indications for this instrument?
These ortho bird beak pliers are indicated for all oral surgery and orthodontic procedures requiring the bending of fine wires. They are particularly useful during stabilization or retention steps in guided bone regeneration (GBR) protocols. Their design allows for the formation of precise loops and sharp angles without weakening the wire material. The use of these fine bird beak pliers is strictly reserved for qualified healthcare professionals, such as dental surgeons and orthodontists, operating in clinical contexts where space management and arch tension are critical to treatment success.
What are the technical characteristics of the Hu-Friedy pliers?
The precision bird beak pliers are distinguished by their ability to handle wires up to 0.020 inch. Their design by Hu-Friedy Mfg. Co., LLC is based on advanced engineering offering perfect jaw symmetry for homogeneous force transmission. Although specific materials are not detailed in the provided technical documentation, this Class I instrument is calibrated to offer adequate resistance during repeated forming. Its thinness allows access to restricted areas of the oral cavity, thus facilitating direct intra-oral adjustments or laboratory work on precision models.
What are the contraindications for the use of this device?
According to information provided by the manufacturer Hu-Friedy, specific contraindications are not exhaustively listed outside of the intended use. However, using the instrument on wires exceeding the maximum capacity of 0.020 inch is prohibited, as this could damage the pliers' jaws or alter bending precision. It is imperative that the user respects standard sterilization and maintenance protocols for reusable medical devices. Any use diverted from its function of forming fine orthodontic wires could compromise the integrity of the instrument and patient safety during the intervention.
What are the maintenance precautions for these non-resorbable pliers?
As a non-resorbable metallic instrument, the Hu-Friedy pliers require a rigorous decontamination and sterilization protocol after each intervention. Before the first use and between each patient, the practitioner must refer to the instructions for use to guarantee the tool's longevity. It is advised to check the alignment of the jaws and the absence of bonding material residues or corrosion. Particular attention must be paid to cleaning the joints to maintain fluidity of movement. Compliance with these precautions ensures that the pliers retain their gripping and bending properties necessary for fine surgery procedures.
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. This product is classified as a Class I medical device, in accordance with the regulations in force for manual surgical instruments. Although the specific CE marking is not mentioned in the source data, the manufacturer is internationally recognized for its compliance with strict quality standards. It is essential for the healthcare professional to read the instructions carefully before any use to ensure the compliance of the procedures implemented with the Hu-Friedy manufacturer's recommendations.
State of the art
Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.
Specifications
| Manufacturer | Hu-Friedy |
| Tags | |
|---|---|
| Tags | |