10ml REIN PRP Single Vacutainer Tube - 1 pcs

⭐ UDB 10ml Rein PRP Single Vacutainer Tube

Precision-engineered for reliable PRP extraction

The UDB 10ml Rein PRP Vacutainer is the ideal solution for clinics and practitioners starting their PRP journey or working with lower treatment volumes. Designed for medical-grade performance, this single-use vacuum tube ensures consistent platelet-rich plasma separation with every draw.

Crafted with CE-certified materials and pre-loaded with a clinical anticoagulant, it preserves platelet integrity from collection to centrifuge — giving you cleaner layers, better concentration, and superior treatment outcomes.

Perfect for face, hair, and joint PRP protocols, this single 10ml tube offers flexibility and affordability without compromising safety or results.

Whether you’re adding PRP to your menu or topping up supplies, the UDB PRP Single Tube delivers the purity, sterility, and clinical confidence professionals expect.

Key Features
✔ 10ml premium PRP vacutainer
✔ Sterile, sealed & CE-certified
✔ Supports high platelet yield
✔ Ideal for clinics trialling PRP or low-volume treatments
✔ Cost-effective without sacrificing quality

Reliable PRP starts with the right tube — choose Uptodatebeauty for clarity, consistency, and confidence.

REIN PRP Tubes are a vacuum tube containing 1 ml of sodium citrate. Ideal for Hospitals, Clinics, Branch Centers where the supportive medical supplies required for treatment are available. It has been designed and approved to enable you to provide appropriate
treatment to patients The sodium citrate used in REIN PRP Kits has a CE certificate, 3,13% Ph. Eur. or 3.8% Erg.-86. It is a high quality component with value. All of our products are produced in our facilities, which have a clean room in accordance
with “ISO Class 8” standards, and it is also confirmed by current validation measurements, without leaving aside our high quality.

Our kits are approved by the notified body (2195) and certified with a CE Class IIB certification by Notified Body/ According to Annex II (excluding section 4), Section 3 of the directive 93/42/EEC on medical devices. Also our product performances are measured by regular tests by independent organizations.