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PRP Centrifuge Medifuge
The Medifuge PRP centrifuge from Silfradent is specifically designed for the production of Platelet Rich Plasma (PRP) and Platelet Rich Fibrin (PRF) with PRP tubes and offers fractionated centrifugation with a preset 6-part program.
This specially designed centrifuge provides everything you need for efficient platelet and growth factor yield. With the preset 6-part program and PRP tubes, fractionated centrifugation is a breeze.
But that's not all: the Medifuge PRP centrifuge is also a Class IIa medical device, which means it meets the highest quality standards and is suitable for professional medical use.
PRP centrifuge - Medifuge
The Medifuge PRP centrifuge from Silfradent - the ideal solution for the production of Platelet Rich Plasma (PRP) and Platelet Rich Fibrin (PRF).
Effective recovery of platelets and growth factors is achieved by centrifugation. Here, the relative centrifugal force plays a decisive role, which depends on the size of the rotor. We work according to the most current protocol, which recommends the use of low RCF. This is confirmed by two recently published studies. The Medifuge is the standard for PRP therapies in 80 countries worldwide.
It is important to note that only centrifuges certified as a class 2a medical device may be used for the production of PRP (platelet-rich plasma). Such certification is held by the Medifuge PRP centrifuge, which also has a sterilization cycle to prevent cross-contamination. The use of PRP/PRF in medicine requires the use of a "practice centrifuge," which are commonly referred to as centrifuges used for therapeutic treatments, such as the preparation of autologous blood preparations. Therefore, these centrifuges are classified as class 2a medical devices. The Medifuge CGF PRP centrifuge meets these requirements.
- The MEDIFUGE CGF's microprocessor control system allows it to maintain a constant speed, ensuring precise separation of blood samples.
- The exception rotor system with self-ventilation protects the blood sample from heat exposure and ensures safe operation. The rotor holding compartment, lid, and test tube holders are especially designed for biological safety in the event of test tube breakage.
- The test tube holders and rotor are made of thermal, anti-static material that is easy to clean, extract and sterilize. MEDIFUGE CGF is equipped with a decontamination cycle with UVC-reflected light, which ensures the safety and cleanliness of the instrument.
- The electronic control motor and its internal parts are maintenance-free and do not require regular maintenance.
- The noise level is extremely low and falls below the required standards. It does not exceed 57 dBa, which ensures a pleasant working environment.
General description
The MEDIFUGE CGF is a powerful and versatile centrifuge that can be operated directly for maximum ease of use. It is the result of close collaboration with experienced dentists and surgeons and careful study of current technological innovations in the electromechanical and electronic fields.
The rotor and the inclination of the tubes are designed to achieve excellent results. The instrument is designed to operate only with the original rotor and test tube holder, and has two operating cycles for centrifugation of blood to obtain fibrin concentration and fibrin clots.
The motor is protected by the control card with current and voltage control to avoid electrical overload. If the machine or control card fails, the lid will remain closed until the rotor stops to ensure safety.
Video
Application area
- Orthopedic surgery
- Maxillo facial surgery
- Oral surgery
- Ophthalmology
- Cosmetic surgery
- Sports Medicine
- Dermatology
- Gynecology
- Neurosurgery
Technical features
- Power source: 230V +/- 10% | 50/60 Hz
- 100-115 V 50/60 Hz;
- Rated power consumption: 120 VA;
- Weight: 9.4 kg;
- Dimensions: 230 PX 320 LX 240 H.
93/42/EEC (Annex II) CE 0051
The CE declaration of conformity is valid for the MEDIFUGE CGF system, which includes centrifuge + kit for the preparation of CGF.
Certificate n. 928 / MDD CE CERTIFICATE Declaration of Quality System Approval (Full Quality Assurance System) SILFRADENT SRL 47018 SANTA SOFIA (FC) - VIA GIUSEPPE DI VITTORIO 35/37 (ITA) - Italy In view of the results of the controls carried out in accordance with Annex II, maintains in the factories of: 47018 SANTA SOFIA (FC) - VIA GIUSEPPE DI VITTORIO 35/37 (ITA) - Italy
Rotor load
To ensure proper balance and avoid possible damage to the blood components due to vibration, it is important to insert the tubes in pairs and in opposite holders, as shown in the figure, to balance the rotor.
Scope and use
Description of the CGF
It is the desire of every surgeon to have access to materials that heal wounds and prevent all secondary effects of surgical procedures (edema, dehiscence, infections, hematomas, etc.). Growth factors are molecules that can specifically activate these processes. They can be natural or synthetic. The peculiarity of GF (Growth Factors) is their excellent reactivity even at very low concentrations. In fact, we are on the order of micrograms. It is certainly better to obtain GFs directly from the patient's tissue. Blood is the donor tissue that is easiest to handle.
The best known GF extraction techniques are:
- fibrin sealant (Tissucol Baxter)
- cPRP platelet concentrate (Marx 1998)
- Platelet-rich plasma (PRP)
- Plasma rich in growth factors (PRGF E. Anitua)
- Fibrin-rich plasma (2001 J. Choukroun)
- CGF (Concentrated Growth Factors IAIO2006,)
The C.G.F. (Concentrate Growth Factors) is a reparative biomaterial comparable to the platelet and fibrin concentrate, enhancing the properties of this technique. The autologous matrix consists of a fibrin block and a platelet concentrate, with a large amount of:
- Plasma cytokines
- platelets: Platelets
- Activated fibrin
- Leukocytes
- GF
- Antibody
Special biological properties of C.G.F.:
- Blood coagulation with formation of a flexible and elastic fibrin network.
- Neoangiogenesis (promotion of vascularization and graft survival)
- Cytokine activation in plasma
- Local activation of the immune system
- Release of GFs from platelet disaggregation and fibrin concentration.
CGF-induced processes:
- Angiogenesis
- Inoculation
- Proliferation of fibroblasts and osteoblasts.
- Repair stimulation and modulation Structural and mechanical properties of CGF:
- Slow and natural polymerization leads to physiological thrombin concentration.
- Trimolecular and Multiple Fibrin Monomer Compounds
- The thin, soft, elastic and permeable network allows the settlement of reparative cells, red and white blood cells, platelets and antibodies.
C.G.F. is prepared by drawing the patient's blood in 10 ml glass PV 200R tubes and centrifuging immediately with the MEDIFUGE CGF from Silfradent S.r.l.. Two to eight tubes can be collected and centrifuged simultaneously.
A single centrifugation without addition of other substances results in fractions in each tube. A lower portion containing all red blood cells, an upper portion containing platelet-poor plasma (PPP), and a fibrous clot between these two fractions that is removed from the tube and separated from the red fraction with scissors.
The clot can be used in the form of a membrane by pressing it or grinding it into smaller fragments. MEDIFUGE CGF centrifuges from Silfradent S.r.l. with the kit accessories are designed for processing blood to obtain C.G.F. in a sterile environment to avoid contamination of the implant material. Any other use is not allowed.
The MEDIFUGE CGF is a centrifuge for dentistry, cosmetic surgery and general surgery.
This centrifuge must be used in combination with the selected or specially developed accessories of this kit to obtain blood clots and blood components for use in the clinic:
- Periodontics
- implantology
- Oral and maxillofacial surgery
- cosmetic surgery
- general surgery
- healing of ulcers
- healing of wounds.
The environment in which the centrifuge is used must have a maximum temperature between and20 °C, 25because the separation of the blood to obtain the CGF must take place within this temperature range.
ATTENTION!Sale only to qualified personnel and their purchasers; take into account the legal regulations on medical devices and their use.
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