Listing Guidelines

DigimedExpo operates as a medical technology marketplace, digital expo, procurement, advertising, community, event, newsletter, and e-magazine ecosystem.

All listings, adverts, RFQ responses, live events, product launches, expo records, community posts, and uploaded documents must follow applicable laws, industry standards, and platform policies.

Non-compliance may result in immediate removal of listings, suspension, or legal action.

Users are encouraged to report non-compliant or fraudulent listings.

Listings must provide accurate and truthful descriptions of the product, spare part, or technology.

Mandatory details such as country of origin, brand, category, warranty period, short summary, and condition must be included.

Advertisements must be regularly updated to reflect the exact specifications.

Banner ads, featured expo placements, and product launch promotions must use truthful, medically appropriate, high-quality creatives and destination links.

DigimedExpo may reject, pause, or remove promotional content that is misleading, low quality, non-medical, unsafe, or inconsistent with the selected placement.

Only legally authorized company logos may be used.

Unauthorized third-party logos are strictly prohibited.

Images must accurately depict the product, spare part, or technology being listed.

Altered images containing additional text, watermarks, or overlays are not permitted.

Sellers must ensure they hold rights to all images used.

High-quality images are strongly recommended for clarity and trustworthiness.

Only non-pharmaceutical medical products may be listed.

All products must meet certification requirements such as FDA, CE, ISO, GMP, or KEBS approvals.

Used medical devices must be sold in their original condition with accurate descriptions.

Listings should include official documentation such as user manuals, certifications, and labels.

Claims about diagnosis, treatment, performance, safety, or regulatory approval must be supportable and must not overstate what the documentation proves.

Pharmaceutical products, controlled substances, and unapproved drugs must not be listed.

Counterfeit, stolen, or black-market items are prohibited.

False, misleading, or exaggerated advertisements are not allowed.

Items that violate intellectual property rights are prohibited.

Users must comply with national and international regulations governing medical devices.

Any unethical business practices, fraud, or misrepresentation will lead to an immediate ban.

Do not publish public prices, buyer budgets, or procurement promises in ways that undermine fair sourcing or expose sensitive commercial information.

DigimedExpo supports discovery and communication, but users remain responsible for due diligence, contract decisions, import/export compliance, and professional judgment.

Community discussions, answers, mentions, and comments must be professional, truthful, relevant, and respectful.

Live events, webinars, product launches, and expo pages must clearly represent the host, topic, timing, and intended audience.

AI-assisted content must be reviewed by the user before publication and must not be used to fabricate certifications, clinical claims, testimonials, or supplier credentials.

Newsletters and e-magazine snapshots may feature marketplace content, but private buyer details, restricted lead information, and confidential procurement data must not be exposed.