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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


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

Blood collection butterfly with retractable needle

Blood collection butterfly with retractable needle and holder.

  • 21G x 3/4"
  • Single use
  • Non toxic

A-PRF Red Tubes

A-PRF Red Tubes are sterile, plain vacuum tubes without additives, anticoagulants, or gels, intended for the preparation of Solid Platelet-Rich Fibrin (A-PRF) from autologous blood. They are specifically designed to facilitate the preparation of PRF clots and membranes for clinical use.


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