Dental PRF Box GRF System – Surgery Membrane Kit CE Certified
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100% Autoclavable & Passivated AISI 420 SteelSKU: SP-85491
OR & Quality SpecificationsHospital Grade
Steel MetallurgyGerman AISI 420 Martensitic
Sterilization Cycle134°C / 273°F Steam Autoclave
Quality StandardISO 13485:2016 & CE Mark
Optical FinishAnti-Glare Satin Matte
Electrochemical PassivationCSSD Laser Batch Tracking
General Surgery InstrumentsSKU: SP-85491AISI 420 Martensitic

Dental PRF Box GRF System – Surgery Membrane Kit CE Certified

4.9 / 5.0•18 Verified OR Evaluations
$360.00$400.00/ unit

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The Dental PRF Box GRF System is designed to support the preparation and handling of platelet-rich fibrin (PRF) membranes for dental and oral surgery applications. Its box-style system helps organize the membrane preparation process, while the included components should be verified against the supplier’s specifications before use.

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The Dental PRF Box GRF System is a dental surgical kit designed to assist with the preparation and handling of platelet-rich fibrin (PRF) membranes. PRF is an autologous fibrin material prepared from a patient's own blood using an appropriate processing protocol. In dental and oral surgery settings, PRF membranes may be used as part of selected clinical procedures according to the treating professional's judgment and the applicable product instructions.

A dedicated PRF box system provides an organized workspace for handling the prepared fibrin material. Its design is intended to help dental professionals manage the membrane preparation process in a more controlled and consistent manner. The exact workflow, instruments, and accessories included depend on the configuration supplied with the kit.

Purpose and Dental Applications

PRF membrane systems are used in professional dental settings where platelet-rich fibrin is prepared for clinical use. Potential applications may include selected oral surgical procedures, periodontal treatment, implant-related procedures, and other applications specified by the manufacturer. The suitability of PRF for a particular procedure depends on the patient's needs, the clinician's assessment, and the applicable clinical protocol.

The GRF system name should be verified against the manufacturer's product documentation because naming conventions and included components can vary between suppliers. Buyers should confirm whether the kit is intended specifically for PRF membrane preparation and whether it includes a compression box, collection accessories, or other instruments.

Design and Handling

The box-style format is intended to provide a designated area for handling the fibrin material during membrane preparation. Depending on the supplied configuration, the system may include a box, compression plate, collection tray, or related accessories. These components must be confirmed with the supplier rather than assumed from the product title alone.

A well-organized preparation system can help clinicians keep the workflow orderly and handle the material according to the manufacturer's instructions. Correct use requires appropriate training, suitable blood-processing equipment where applicable, and adherence to established infection-control procedures.

Materials and Construction

The product title does not specify the material, dimensions, or construction of the box and accessories. These details should be confirmed before ordering, particularly if the kit will be used in a clinical environment. The buyer should also verify whether the supplied components are reusable or single-use and whether any reusable parts are compatible with the facility's validated cleaning and sterilization procedures.

CE Certification and Quality Verification

The product is described as CE certified in the supplied title. Before purchasing, request the applicable Declaration of Conformity, device identification, manufacturer information, and supporting documentation to verify the certification claim and intended use. CE marking requirements and documentation depend on the product's regulatory classification and market.

Cleaning, Sterilization, and Storage

Follow the manufacturer's instructions for cleaning, disinfection, sterilization, and storage. Do not assume that every component is autoclavable or suitable for repeated use. Confirm the approved processing method, temperature limits, and expected service life for reusable parts. Maintain appropriate aseptic handling throughout preparation and clinical use.

The Dental PRF Box GRF System is intended for professional use where its documented configuration and instructions match the requirements of the dental practice. Confirm the kit contents, material, dimensions, reuse status, and compatibility with the intended workflow before ordering.

Key Features

  • Designed for PRF membrane preparation and handling

  • Intended for professional dental and oral surgery workflows

  • Box-style format for organized material handling

  • May support selected periodontal and implant-related procedures when clinically appropriate

  • Kit configuration depends on the supplier's specification

  • Material and dimensions require manufacturer confirmation

  • Reusability and sterilization method must be verified

  • Intended use should be checked against product documentation

  • CE certification claim should be supported by valid documentation

  • Suitable for procurement by dental clinics and professional practices after verification

Product Specifications

SpecificationDetails
Product NameDental PRF Box GRF System
Product TypePRF membrane preparation kit
SpecialtyDental and oral surgery
Intended PurposePreparation and handling of platelet-rich fibrin membranes, subject to manufacturer instructions
System FormatBox-style system
Included ComponentsConfirm with supplier
MaterialConfirm with supplier
DimensionsConfirm with supplier
CE CertificationAdvertised as CE certified; verify supporting documentation
Reusable or DisposableConfirm with manufacturer
Cleaning and SterilizationFollow validated manufacturer instructions
CompatibilityConfirm with the intended PRF preparation workflow
Country of OriginConfirm with supplier

Frequently Asked Questions

1. What is a Dental PRF Box GRF System?

It is a box-style dental kit intended to assist with preparing and handling platelet-rich fibrin membranes. The exact components and workflow depend on the manufacturer's configuration.

2. What is a PRF membrane used for in dentistry?

PRF membranes may be used in selected dental, periodontal, and oral surgical procedures. Their use depends on the clinical indication, professional judgment, and applicable instructions.

3. What comes with the Dental PRF Box GRF System?

The included parts are not specified in the product title. Ask the supplier for a complete component list and product images before ordering.

4. Is the Dental PRF Box GRF System CE certified?

The title advertises CE certification. Request the relevant Declaration of Conformity and product identification details to verify the claim.

5. What material is the PRF box made from?

The material is not specified. Confirm the material and its suitability for the intended clinical environment with the manufacturer.

6. Can the PRF box be autoclaved?

Autoclave compatibility cannot be confirmed from the title alone. Follow the manufacturer's validated cleaning and sterilization instructions for each component.

7. Is this kit reusable?

The reuse status is not specified. Confirm which components are reusable, which are disposable, and the approved reprocessing procedure.

8. Can this system be used for dental implant procedures?

PRF may be used in selected implant-related workflows when clinically appropriate. Verify that the system is intended for the planned application and follow the manufacturer's instructions.

9. Does the kit include a centrifuge?

The title does not indicate that a centrifuge is included. Confirm the complete kit contents and any required compatible equipment before purchase.

10. What should I check before purchasing this PRF membrane kit?

Verify the complete contents, dimensions, materials, intended use, compatibility, reusability, sterilization instructions, manufacturer details, and supporting CE documentation.