CDM Cartridges. Disposable
Sterile Path
for AXIONOVA AXIS.
CDM cartridges are the disposable drug-path modules for AXIONOVA AXIS. Each cartridge is designed for single-use sterile workflow, keyed quarter-turn bayonet seating, NFC identity verification, needle safety, and ALETHRA-governed chain-of-custody records.
The reusable AXIS body never contacts the drug product, sterile path, or needle path. The cartridge carries the sterile boundary. AXIS provides the reusable mechanical, electronic, verification, and governance layer around it.
One cartridge.
One identity.
One governed use event.
The CDM cartridge is not a simple container. It is a disposable module that links physical material, compound identity, cartridge status, sterile pathway, needle workflow, and digital authorization.
Each cartridge seats into AXIS through a quarter-turn bayonet interface. The geometry is keyed for single-orientation placement. Once seated, AXIS verifies the cartridge through NFC and confirms mechanical lock through axial and rotational sensors before the workflow can proceed.
Cartridge specifications.
Every CDM cartridge is structured for single-use sterile workflow, keyed seating, NFC identity verification, dual lock confirmation in AXIS, and ALETHRA-linked use-state records.
The cartridge is verified
before the event.
Every CDM cartridge carries an NFC identity that AXIS reads before use. ALETHRA connects that identity to the compound record, lot information, release status, access eligibility, use state, and event history.
This prevents the cartridge from being treated as an anonymous consumable. The cartridge is part of a governed record across compound, unit, practitioner access, AXIS device identity, and delivery workflow.
The reusable device stays
outside the drug path.
AXIONOVA separates reusable intelligence from disposable sterility. The AXIS body contains the durable mechanical and electronic platform. The CDM cartridge contains the single-use sterile drug path and needle workflow.
CDM cartridges and needles are disposable and intended for single-use workflows. Needle handling, use, and disposal are managed under practitioner and qualified research protocols. AXIONOVA does not position cartridges or needles for consumer self-selection or direct-to-consumer ordering.
From release to disposal,
every step is governed.
AXIS verifies cartridge seating and identity before workflow progression. ALETHRA records the cartridge event so partner teams can maintain device, cartridge, and chain-of-custody documentation.
CDM cartridges are for controlled research-use workflows through verified practitioner and qualified research channels. AXIONOVA does not sell cartridges directly to consumers. Final use, claims, and regulatory status depend on applicable jurisdiction, intended use, validation status, and partner responsibilities.
Disposable sterile path.
Reusable governed instrument.
CDM cartridges and AXIS work together to keep the sterile path inside the disposable module while the reusable AXIS body governs identity, authorization, lock state, dose verification, and event records.