Replacement for BLPG crown lengthening gauge - Hu-Friedy - Delynov
The Recharge pour jauge allongement de couronne BLPG - 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 BLPG crown lengthening gauge refill?
The BLPG crown lengthening gauge refill is a replacement component designed by Hu-Friedy, a recognized manufacturer in the field of periodontal instrumentation. This device is inserted into the frame of measuring instruments used to quantify the biological space required during corrective surgeries. As part of the consumable category (CONSO), this refill allows for the maintenance of clinical measurement reliability without having to replace the entire handle or instrument support. Its design is specifically adapted to Hu-Friedy brand requirements to guarantee perfect compatibility and precise reading of clinical parameters during interventions.
What are the clinical indications for this device?
This device is indicated during aesthetic dental surgery interventions requiring clinical crown lengthening. It is used by the periodontist or dental surgeon to accurately measure the distance between the cemento-enamel junction (or the edge of the future prosthesis) and the alveolar bone crest. This step is crucial for respecting the biological width and preventing chronic post-restorative gingival inflammation. The use of an aesthetic dental surgery probe like the BLPG gauge allows for predictable guidance of osteotomy and osteoplasty, thus ensuring long-term soft tissue stability after the placement of crowns or veneers.
What are the technical characteristics of this refill?
The BLPG refill is manufactured by Hu-Friedy Mfg. Co., LLC according to rigorous quality standards. Although detailed material specifications are not explicitly listed, this product belongs to Class I of medical devices, which corresponds to non-invasive or temporary invasive instruments presenting a low risk. The refill is designed to mechanically fit the corresponding crown lengthening gauge, allowing for a clear reading of the graduations necessary for periodontal evaluation. As a surgical periodontal probe, it must meet the sterilization and durability requirements specific to demanding clinical environments, while maintaining the integrity of its markings for constant precision.
What are the contraindications for the use of this product?
According to the data provided by the manufacturer Hu-Friedy, there are no specific medical contraindications listed for this refill, other than those related to the periodontal surgical procedures themselves. However, the use of this device is strictly reserved for qualified healthcare professionals. It is imperative not to use the product if it shows signs of degradation or if compatibility with the gauge handle is not ensured, as this could distort clinical measurements. Practitioners must systematically refer to the instructions for use before any manipulation to ensure compliance with the safety and hygiene protocols in force in their practice or clinic.
What are the precautions for use and maintenance?
As a Class I device, the crown lengthening gauge refill must be handled with care to avoid any deformation of the measuring tips. Before the first use and between each patient, the device must be cleaned and sterilized in accordance with the instructions from the manufacturer Hu-Friedy. It is essential to check the condition of the graduations; any wear making reading difficult must lead to the immediate replacement of the refill to guarantee the safety of care. Although it is not a suture, the precision of this surgical periodontal probe is decisive for the success of aesthetic dental surgery and the respect of the patient's periodontal anatomical structures.
Who is the manufacturer and what standards are respected?
The official manufacturer of this medical device is Hu-Friedy Mfg. Co., LLC, located in Chicago, USA. This product is classified as a Class I medical device, which implies that it meets the basic regulatory requirements for this category of instruments. The manufacturer emphasizes that the use of this equipment is strictly reserved for healthcare professionals. Although specific CE marking is not mentioned in the source data, compliance with Hu-Friedy manufacturing standards ensures consistent quality. Practitioners are invited to read the instructions for use carefully to understand all warnings and the maintenance protocols recommended by Hu-Friedy in order to guarantee the longevity of the instrument.
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Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Hu-Friedy |
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