IMS Endo 24 Instrument Sequencer - Hu-Friedy - Delynov - Online Store
The IMS Séquenceur Endo 24 instruments - 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 is the IMS Endo Sequencer 24 instruments - Hu-Friedy - Delynov?
The IMS Endo Sequencer 24 instruments, designed by Hu-Friedy, is a specialized organization device for managing root canal instruments. This endo instrument holder allows for maintaining up to 24 instruments in an orderly and secure manner. It integrates into the practice's sterilization and organization protocol, providing a rigid structure to prevent mixing files during clinical procedures. As a component of the IMS (Instrument Management System), this endodontic sequencer helps standardize the preparation of technical trays, ensuring that each instrument is in its place before, during, and after the intervention.
What are the clinical indications for this endodontic instrument holder?
This endodontic instrument holder is indicated for all phases of endodontic treatment, from coronal access to obturation. Its primary use lies in the sequential organization of manual or rotary files required for canal reaming. In dental surgery and endodontics, it allows the practitioner to precisely track their instrumental progression. The use of this endodontic sequencer is particularly recommended during complex treatments requiring a large number of different instruments, thereby minimizing handling errors and increasing efficiency during root shaping.
What are the technical characteristics of this Hu-Friedy sequencer?
The Hu-Friedy sequencer is specifically sized to accommodate a complete series of 24 instruments. Its design allows for easy insertion and removal of files while ensuring they are held securely during cleaning cycles. Unlike a standard endodontic cassette, this model focuses on the vertical or tilted presentation of instruments for immediate visual identification. Manufactured by Hu-Friedy Mfg. Co., LLC, this device meets the durability requirements necessary to withstand repeated decontamination and autoclave sterilization processes, ensuring longevity in line with the brand's standards.
What are the contraindications for the use of this device?
According to the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, there are no specific medical contraindications related to the use of this holder. However, its use is strictly reserved for qualified healthcare professionals. It is imperative to follow validated sterilization protocols to avoid any risk of cross-contamination. Users must ensure that the inserted instruments are compatible with the dimensions of the sequencer to avoid any damage to the equipment or the files themselves. Regular inspection of the device is advised to check for any structural degradation.
What are the precautions for use for this non-resorbable material?
As this is an instrument management device and not an implant, the concepts of resorption do not apply. However, rigorous precautions must be observed regarding maintenance. The practitioner must read the instructions carefully before use. The sequencer must be cleaned and sterilized before the first use and between each patient. Instruments should be handled with care when being inserted into the endo instrument holder to avoid accidental needle sticks. Storage in a dry and clean environment after sterilization is necessary to maintain the integrity of the device and the instruments it contains.
Who is the manufacturer and what standards are met?
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 according to current regulations. As a recognized manufacturer in the dental sector, Hu-Friedy guarantees that this sequencer meets the quality and safety standards applicable to reusable instruments. Compliance with Class I highlights that this device presents a low level of risk and is intended for supervised professional use. Users are encouraged to systematically refer to the manufacturer's instructions to ensure use in accordance with regulatory requirements.
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Specifications
| Manufacturer | Hu-Friedy |
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