Product Description
What this is and who it's for
Revital‑Ox RESERT is a ready-to-use hydrogen‑peroxide based high‑level disinfectant intended for the reprocessing of semi‑critical medical devices (for example flexible endoscopes and ultrasound probes). It is supplied in 4 L bottles and is sold for clinical and institutional use by Steris and authorized distributors.
Specifications
- Net contents: 4 L per bottle as sold in the 4440AWCA Canada pack (4 × 4 L per case).
- Active chemistry: 2% Accelerated Hydrogen Peroxide (AHP) as stated in manufacturer materials.
- Reuse: manufacturer IFU permits reuse undiluted for up to 21 days provided minimum concentration is confirmed with the Revital‑Ox RESERT R60 test strip before each use.
- Intended processing: manual soaking or open‑architecture automated endoscope reprocessors (manufacturer guidance).
What is included / commonly sold
- - A single 4 L ready-to-use bottle (many sellers list this item as the EA unit); the manufacturer product number 4440AWCA is supplied as a pack of four 4 L bottles (4 each / case).
- - R60 solution test strips are a separate consumable (sold separately) and are required to verify minimum concentration when reusing solution.
Condition and packaging
- - Product is sold new, factory packaged; 4440AWCA is listed as the Canada-only 4×4 L case on Steris ordering pages.
Usage notes
- - Follow the Steris Instructions For Use exactly: the Steris IFU and technical documentation state a minimum immersion/contact time of 8 minutes at ≥ 20°C for high‑level disinfection and detail reuse/monitoring requirements.
- - Rinse and handling: the IFU and distributor instructions specify rinsing requirements; follow the IFU for rinse duration and water quality.
Limitations and warnings
- - Conflicting contact-time claims exist in reseller listings (some Canadian resellers advertise a 5‑minute contact time for SKU 4440AWCA). The Steris IFU/technical specification documents state an 8‑minute minimum immersion time at ≥ 20°C — do not rely on reseller text when protocols or regulatory compliance is at stake; follow the Steris IFU and local policy. See warnings below.
- - This product is a high‑level disinfectant (HLD), not a sterilant. Users must follow device manufacturer and local regulatory reprocessing requirements.
If you need copies of the Steris Instructions for Use, COA or SDS these are available from the manufacturer; verify the contact time and rinse procedure directly against the Steris IFU before use.
Product Videos
Custom Field
BBMProdID BBM01
