RSA™ (Reduced Surface Activity) autosampler vials are manufactured pyrogen free. During production, the vials are formed under sterile conditions and are never exposed to human contact. Following fabrication, they are assembled and shrink‑wrapped within a Class 10,000 clean‑room environment, ensuring controlled bioburden and particulate levels throughout packaging.
Although the vials themselves are produced under sterile conditions, they are not sold as a sterile product, as the final packaging is not terminally sterilized. However, the cleanliness of the manufacturing workflow provides a strong baseline if end‑users intend to apply their own sterilization procedures.
All manufacturing processes for RSA vials are conducted under ISO‑certified quality systems, ensuring consistent control of contamination, materials, and handling. For additional technical details on RSA vials, inserts, and closure systems, please refer to our product documentation.
More information about RSA vials, inserts and caps
