Quality & Evidence
Kejulong does not use one report to describe every model. Testing, safety and transport information is reviewed against the intended product, destination market and customer requirement.
Public Evidence Groups
This page explains document categories and boundaries. It does not replace the report file or a product-specific review.
Selected submitted black and white food-container masterbatch samples have test records for specified GB 9685-related items.
Boundary: The record applies only to the submitted sample and tested items. It is not a blanket statement for every model.
Selected submitted samples have records for specified GB 4806.7 sensory and migration test items.
Boundary: The final article, dosage, contact condition and destination requirement must still be confirmed.
Selected submitted black and white food-container masterbatch samples have records for specified 21 CFR 177.1520 extraction-related items.
Boundary: This is not described as a generic FDA certification.
Selected submitted samples have records for specified EU POPs, REACH and RoHS items.
Boundary: A result for listed substances must not be expanded to an unsupported all-substance or all-model claim.
SDS and selected sea-transport condition documents can support customer documentation where applicable.
Boundary: An SDS is not a product certification, and a transport document applies only to the listed sample and transport condition.
Review Workflow
The review begins with the exact product and intended use, not with a general marketing phrase such as food grade or certified.
Confirm the model, sample, color, production route and intended application before matching any document.
Confirm the destination market, final article, contact condition and the customer's specified test items.
Use only a report or document that covers the relevant submitted sample and test scope.
Where existing evidence does not cover the requirement, agree on the sample and test project before submission.
Public and commercial statements remain linked to the tested item, sample, condition and report conclusion.
Trial Records
A useful record makes repeat evaluation possible and prevents a result from being expanded beyond its tested conditions.
Raw-material and product identification
Sample and customer reference
Resin, dosage and processing conditions
Appearance and color comparison
Application or finished-part trial result
Requested third-party test scope
Approved sample and version record
FAQ
No. Existing records cover specific submitted samples and test items. The exact product model, final use, dosage, contact condition and destination requirement must be reviewed.
It means the product model, submitted sample, destination market and requested test items are confirmed first, and then the test is arranged. It does not mean the product has already passed before testing.
No. Additive-use review and finished plastic article requirements address different scopes. The final PP container or other article must be evaluated for the actual composition, dosage and contact conditions.
No. An SDS communicates safety information. It is not a certificate of conformity or a third-party performance report.
Relevant documents can be discussed after the product, application and requested scope are confirmed. Personal or commercially sensitive information may be redacted where necessary.
Provide the product direction or model, resin, dosage, final application, destination market, contact condition and required test items. We will review the relevant scope before supplying a statement or arranging additional testing.
Request Document Review