Time and accuracy matter in the operating room, which is why every ready-to-administer OR Syringe and IV bag from Fagron Sterile Services is thoroughly tested. No syringe is released from quarantine until all testing for sterility, particulate matter, and potency is complete and approved by our Quality team.
All OR Syringes are clearly labeled, adhering to ASTM, DQSA, and ISMP medication and anesthesia labeling standards. This includes TALLman lettering, presentation specifications, barcodes, expiration dating, and storage requirements.
OR anesthesia solutions are produced with cGMP (21 CFR 210 & 211) compliant operations in our state-of-the-art 503B outsourcing facilities to support a reliable supply of medications and our commitment to patient safety.