PRF Seals and Labels for Steribox Large
Steribox® pins and labels
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
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
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
PRF System Starter
PRF System Starter
Our carefully selected PRF Starter kit is designed for clinicians who are beginning their use of Platelet-Rich Fibrin in oral surgery, implantology, and regenerative dentistry. It provides all the essential components to confidently perform PRF protocols in a safe, reliable, and clinically accurate manner.
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).
See Supporting Research and Clinical Evidence
The kit also includes complimentary access to Dr. Joseph Choukroun PRF Online Course, valued at $1,000 offering in-depth training from the inventor of Process for PRF
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).
See Supporting Research and Clinical Evidence
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