Submit your surgical or dental instrument references, quantity, target market, branding or packaging brief, and document requirements to Dr. Jays International in Sialkot, Pakistan.
Requested features remain unconfirmed until they appear in a written quotation and approved specification. Include drawings or sample details where available.
Private label starts with an existing catalogue reference and asks for buyer-specific marking, labelling or packaging to be reviewed.
OEM or custom involves a different pattern, dimension, tolerance, finish, material, function or set configuration.
These descriptions classify the enquiry. They do not confirm that a requested change is available.
A detailed brief allows each requested feature to be assessed and recorded against the correct product reference.
| Requirement | Include with the RFQ | Confirm before ordering |
|---|---|---|
| Product reference | Name, catalogue reference, drawing number, reference image or sample identifier | Exact product version and accepted scope |
| Pattern and function | Intended use, working-end details, mechanism and required checks | Approved pattern and acceptance criteria |
| Dimensions and tolerances | Annotated drawing, units, critical dimensions and limits | Controlled drawing, revision and measurement method |
| Material and finish | Requested material specification, finish, coating or surface requirement | Accepted material and finish plus supporting documents |
| Instrument marking | Artwork, text, number, size, placement and traceability data | Method, artwork, placement and legibility criteria |
| Packaging and labelling | Pack configuration, artwork, language, barcode and carton requirements | Accepted configuration, responsibilities and approved label |
| Documentation | Exact document name, format, language, legal entity and target market | Availability, scope, issue stage and commercial conditions |
| Quantity and delivery | Quantity by item, order type, destination and requested date | MOQ, pricing basis, timing, shipping terms and delivery basis |
Change control
The order record should identify who reviews and approves each change, including responsibility for design validation, label review, artwork and market-specific documents.
Use these checkpoints to keep the request controlled. The quotation should state which stages apply.
Provide references, drawings or sample details, dimensions, quantities, destination, requested changes, packaging brief and document list.
Record which requirements are accepted, rejected or need more information. A requested feature is not confirmed until it appears in writing.
If a sample or prototype is required, confirm availability, quantity, cost, freight, timing, revisions and approval criteria before work begins.
Approve the applicable drawing revision, product specification, marking artwork, label, packaging, inspection criteria and document list.
Record quantity, MOQ, timing basis, acceptance criteria, approved references and the process for later changes.
Confirm pack configuration, labels, carton details, destination, shipping terms and shipment documents before release.
Ask whether the minimum applies per item, size, finish, marking, packaging format or total order. Also confirm whether initial orders, repeat orders and samples use different minimums, and how quantity changes affect price and timing.
Confirm availability, what the sample represents, quantity, cost, freight, timing, accompanying documents, approval criteria and the effect of revisions. Agree handling, ownership and return terms before shipping a physical reference.
For marking, provide vector artwork, exact text, size, placement, orientation and traceability needs. For packaging, state the unit, inner and outer configuration, quantities, labels, language, barcode format and destination. Availability requires written confirmation.
List the exact specification, drawing, inspection, material, marking, packaging, shipment or market document required. The response should state its scope, issuing entity, language, delivery stage and any restriction.
Review documentation enquiries →Before sharing confidential drawings or unrestricted brand files, request written terms covering access, permitted use, storage, copying, return, destruction, ownership, third-party disclosure and publication permissions.
Until those terms are agreed, send only the information needed for an initial review.
Private-label requests usually start with an existing reference and add buyer-controlled marking, labelling or packaging. OEM requests may also involve pattern, dimensions, tolerances, material, finish or functional changes. Every change remains subject to written review and approval.
You can submit a drawing, specification, reference image or physical-sample description for review. The request is not accepted until a written quotation confirms feasibility, scope, approval stages and commercial terms.
You can include laser marking in the RFQ with vector artwork, exact text, size, placement and legibility requirements. The method and availability must be confirmed for the exact instrument.
No universal MOQ is published. Request an order-specific minimum and confirm whether it applies per item, size, finish, marking, packaging format or total order.
State the requirement in the RFQ. Availability, quantity, cost, freight, timing, approval criteria and revision terms must be confirmed in writing.
Submit the required configuration, artwork, language, barcode format, pack quantity and target-market information. Do not assume a format is available until it is confirmed in the quotation.
Request each document by name. Availability must be confirmed for the exact product, order, target market and legal entity. General website copy is not evidence of certification, registration or conformity.
No public confidentiality or intellectual-property terms are verified in this repository. Request written handling, ownership, access, return, destruction and disclosure terms before sending sensitive materials.
No verified public lead-time range is available. Ask the quotation to state its timing basis and the effect of samples, revisions, quantities, marking, packaging, documents and approvals.
Include the product reference, changes, quantities, target market, destination, packaging brief and named documents. Submission does not confirm availability, customization, MOQ, samples, pricing or timing.
