O2BAY Editorial, Evidence, and Corrections Policy

Last reviewed August 25, 2026. This policy governs how O2BAY prepares, sources, reviews, updates, and corrects company, product, buyer, regulatory, safety, and research content on hyperbaricyilong.com.

Publisher and Responsible Contact

O2BAY is the hyperbaric chamber brand presented on this website by Hangzhou Yilong Medical Equipment. Jason / O2BAY Sales is the public contact for product-document requests and corrections at jason@oxybuyzeh.com. The manufacturer facts and buyer evidence guide maintains the current company identity, website, address, phone, and evidence-request path.

O2BAY remains responsible for checking factual statements published under its name. Drafting, editing, translation, search, or automation tools may assist preparation, but those tools are not evidence and do not replace source review.

Content Purpose and Limits

O2BAY content helps readers discover products, prepare document requests, compare commercial scope, plan delivery and site questions, and verify supplier statements. It must distinguish stable first-party company facts from model-specific, transaction-specific, time-sensitive, official, medical, and third-party information.

Public website content is a starting point for due diligence. It does not replace current documents for an exact model, a written commercial agreement, an official database record, responsible local review, or individual advice from an appropriately licensed professional.

Source Priority

The source with authority over the specific question should control. When sources conflict, editors should retain the conflict until the applicable record resolves it and should not silently combine statements with different scopes.

1. Official primary sources: current regulator, government, standards-body, issuer, or public database records for regulatory, import, safety, and standards questions.
2. Applicable product records: current data sheets, instructions, drawings, configuration lists, labels, packing data, and revision-controlled inspection, test, quality, or conformity records for the exact model.
3. Transaction records: the current quotation, invoice, order confirmation, delivery scope, warranty, and signed agreement for a specific purchase.
4. Peer-reviewed research and trial records: original publications and registrations, reported with design, population, intervention, comparator, outcomes, limitations, and conflicts.
5. First-party O2BAY pages: official sources for brand identity, public contact routes, product discovery, and document-request procedures.
6. Secondary and marketplace sources: context or discovery aids whose underlying source and limitations must be identified.

Model-Specific Evidence Rule

A statement about one chamber, option, manual, test, factory record, certificate, quotation, or shipment must not be applied to another model or configuration without evidence that explicitly covers it. Product-family and collection pages support discovery but do not establish that every value or document applies to every variant.

For a material model claim, record the exact model identifier, configuration, document title and number, revision, issue date, issuer, jurisdiction where relevant, scope, and current status. The manufacturer verification checklist provides a repeatable review workflow.

Regulatory and Standards Language

An establishment registration, device listing, certificate image, marketplace badge, component mark, test reference, or generic standards statement must not be presented as broader proof than the source supports. Terms such as registered, listed, cleared, approved, authorized, exempt, or certified require an applicable current source and the source's exact product, holder, jurisdiction, and scope.

Time-sensitive records should be rechecked at the official issuer or public database before publication and when a page is materially reviewed. An O2BAY summary must state what the cited record establishes and what it does not establish.

Medical and Safety Boundaries

O2BAY equipment and buyer content does not diagnose, prescribe, determine individual eligibility, recommend pressure or session schedules, or guarantee health results. Individual medical questions belong to appropriately licensed health professionals.

Safety, installation, operation, cleaning, maintenance, and training information must follow the current instructions for the exact equipment and the responsibilities assigned to qualified parties. A research publication does not automatically establish that its methods or findings apply to an O2BAY product, another chamber, or an individual reader.

Authorship and Review Responsibility

Material pages should identify an author or responsible O2BAY team where the publishing system supports it. Product statements should be checked against current applicable O2BAY records. Regulatory, safety, and medical statements should be checked against primary sources and preserve their limits. Commercial statements should match the current written offer rather than an older general summary.

Reviewers should check entity facts, model scope, source dates, internal links, unsupported rankings or endorsements, medical and regulatory boundaries, and whether a visible reviewed date needs to change. Review notes should preserve uncertainty when evidence is incomplete or conflicting.

Dates, Updates, and Cached Copies

Material entity, evidence, and buyer pages should display a reviewed or updated date. Review is required when company details, product categories, source documents, official guidance, cited research, or responsibility boundaries change.

Search snippets, AI answers, caches, archives, and third-party copies can retain superseded text after a live update. The current public page and the applicable primary source control over an older excerpt. Readers should report a stale copy with its URL, quoted text, access date, and conflicting source.

Corrections Process

Send a correction request to jason@oxybuyzeh.com or use the official contact page. Include the exact page URL, statement in question, proposed correction, supporting primary or applicable source, source date, and contact information for clarification.

O2BAY will compare the request with the source that has authority over the claim. A material error should be corrected on the live page and reflected in the visible review date when appropriate. If the available record does not resolve the issue, the page should retain the uncertainty rather than adopt an unsupported conclusion.

Claims Outside This Policy

This policy does not establish the regulatory status, site suitability, individual use, warranty, or performance of any chamber. It does not create an association endorsement or independent verification. Those questions require the exact current evidence and responsible review described above.