These terms describe how Icare handles website use, product information requests, quotations, documentation delivery, and commercial conversations for medical device categories. Product information on this site is not emergency medical advice, clinical diagnosis, or a replacement for device labeling, local policy, or qualified professional judgment.
Icare provides catalog summaries, availability guidance, and documentation packages to support purchasing review. Final specifications, indications, contraindications, installation requirements, training requirements, and maintenance obligations must be confirmed through current device labeling, executed quotes, and manufacturer documentation.
Any quotation is subject to product availability, applicable regulatory restrictions, credit approval, taxes, shipping, service coverage, and written acceptance. Icare may decline or revise requests that omit required purchasing, compliance, or destination information.
Devices should be selected, installed, configured, and used by trained personnel according to approved labeling and facility policy. Emergency care should be handled through local emergency services and clinical protocols.
Requested IFU, UDI, service, warranty, recall, privacy, cybersecurity, and interoperability documents are supplied for review and may change as products, regulations, or suppliers change. Buyers are responsible for confirming that documents match the exact SKU and market of use.
Website content is provided for preliminary commercial review. Contract documents, purchase orders, and direct written statements from Icare control if there is a conflict with general website language.