PRF Compactor Small
Brand: PROCESS FOR PRF
PRF Compactor Small allows to compact and tamp the bone filling materials in the recipient sites (alveoli, sinus, goshawks implants).
Related products
I-PRF Purple Tubes
I-PRF Purple Tubes are sterile, plain vacuum tubes without additives, anticoagulants, or gels, intended for the preparation of Immediate Platelet-Rich Fibrin (I-PRF) from autologous blood. These tubes are designed for clinical use in regenerative medicine and aesthetic procedures.
Regulatory Status:
ARTG-listed Class IIa. Official Process for PRF® product, developed by Dr. Choukroun creator of the Process for PRF® (Platelet Rich Fibrin) technique (A-PRF, i-PRF, & S-PRF). CE 0123 The four-digit number indicates the Notified Body responsible for conformity assessment. Devices without a four-digit CE number are not medical devices and must not be used for PRF.
See Supporting Research and Clinical Evidence
Regulatory Status:
ARTG-listed Class IIa. Official Process for PRF® product, developed by Dr. Choukroun creator of the Process for PRF® (Platelet Rich Fibrin) technique (A-PRF, i-PRF, & S-PRF). CE 0123 The four-digit number indicates the Notified Body responsible for conformity assessment. Devices without a four-digit CE number are not medical devices and must not be used for PRF.
See Supporting Research and Clinical Evidence
Expiry date: 04-2027
S-PRF Green Tubes
S-PRF Green Tubes are sterile, plain vacuum tubes without additives, anticoagulants, or gels, intended for the preparation of Liquid Platelet-Rich Fibrin (S-PRF) from autologous blood in dental and medical procedures.
Regulatory Status:
ARTG-listed Class IIa. Official Process for PRF® product, developed by Dr. Choukroun creator of the Process for PRF® (Platelet Rich Fibrin) technique (A-PRF, i-PRF, & S-PRF). CE 0123 The four-digit number indicates the Notified Body responsible for conformity assessment. Devices without a four-digit CE number are not medical devices and must not be used for PRF
See Supporting Research and Clinical Evidence
Regulatory Status:
ARTG-listed Class IIa. Official Process for PRF® product, developed by Dr. Choukroun creator of the Process for PRF® (Platelet Rich Fibrin) technique (A-PRF, i-PRF, & S-PRF). CE 0123 The four-digit number indicates the Notified Body responsible for conformity assessment. Devices without a four-digit CE number are not medical devices and must not be used for PRF
See Supporting Research and Clinical Evidence
For sampling of 8 or more tubes ...use PomCol™
Procedure: Cool the sampler tubing to prevent blood coagulation in the sampler.
https://www.youtube.com/watch?v=0CoeS-p_Tyc
Reviews
There are no reviews yet