For baby brands, importers and wholesale buyers, define the teether design, intended age and destination market before discussing material, samples or a production quotation.
Specify the product's intended age range, selling countries and proposed packaging claims. These inputs help determine classification and the applicable product assessment. Avoid pain-relief or other medical claims without a resolved classification and supporting evidence.
02
Complete design and material
Provide dimensions, wall thickness, texture and any attached parts. Request the exact material and colour specification. Review the finished article and all components; a material report alone does not establish whole-product conformity.
03
Labels and evidence
Include packaging language, brand information, care instructions and traceability requirements. Agree which tests and documents apply to your actual design and market, who provides them and whether they are included in the quotation.
What to send
Target selling countries and intended product age range
Reference drawing or images with dimensions, textures and all parts
Proposed material, colours and packaging claims for review
Brand artwork, packaging languages and documentation requirements
Sample request, estimated order quantity and target launch window
Provide the intended product age range, not child names or personal information.
Design feasibility and exact material / colour / component specification
Product-specific assessment, evidence scope and responsibility for documents
Sample plan, tooling costs, MOQ, quotation and delivery milestones
Buyer questions
Does a silicone material test certify the teether?
No. Identify the tested material and conditions, then determine what assessment and documentation the exact finished design requires. Added parts, colours, labels and intended age can affect the review.
What information is needed for a US or EU project?
Start with the destination market, intended age, complete design and intended claims. Use current official requirements with your compliance team to define the applicable tests and documents. No general US or EU approval is claimed for a reference design.
Are these ready-to-order stock items?
This page supports custom project inquiries rather than confirmed stock SKUs. Samples, material, customization, MOQ, price and delivery timing must be checked against your brief.
Official market references
For baby products, settle intended age, destination market, product classification and proposed claims before agreeing a test and documentation plan with your compliance team. The references below explain regulatory context; they do not certify a Silicraft product.
US: CPSC distinguishes soothing use from teething-pain claims. Its older teether FAQ cites F963-17; the current Toy Safety FAQ identifies F963-23 as applicable from April 20, 2024. Determine the requirements for the exact product.
EU: CE marking is the manufacturer's conformity declaration. A raw-material report or one EN 71 test does not cover the complete article. Regulation (EU) 2025/2509 entered into force on January 1, 2026 and applies from August 1, 2030; plan against the rules applicable when placing the product on the market.