Safety at Every Step

FOR USERS & BENEFICIARIES

RegenLab’s CE-Marked Class IIb Medical Devices are sterile in the fluid path and pyrogen free, thus reducing the risk of contamination. Furthermore, all RegenACR kit components have been tested for biocompatibility, according to ISO 10993 standards.

In order to ensure safety of use, the RegenACR kits are manufactured with double sterile blister packaging and have been designed to be ready for use, without preparation.

CONTRAINDICATIONS

The preparation of PRP must not be administered to patients with hematologic or coagulation disorders, or to patients suffering from serious diseases such as severe metabolic disorders, cancer or acute infection.

The administration of PRP to children, pregnant or lactating women or patients suffering from autoimmune diseases is not recommended.

THROUGH AUTHORIZED RESELLER ONLY

Regen Lab is firmly committed to providing our customers with best-in-class, reliable products through subsidiary companies and authorised distributors

RegenACR is CE Marked and is only available through authorized distributors. The Product has not been approved or cleared for marketing by the United States Food & Drug Administration.