Surgical and dental instrument manufacturing in Sialkot
Dr. Jays International manages manufacturing in-house at its Sialkot facility. Heat treatment is completed by an external process provider.
Review the approved company-level facility, inspection and traceability scope, then prepare an item-specific request.
Approved facility and production scope
The approved company record identifies a co-located office and factory in Sialkot with 6,000 square feet in total. Of that space, 4,500 square feet is allocated to manufacturing.
Toor Abad Daska Road, Opposite Imran Idrees Hospital, Sialkot, Punjab, Pakistan
info@jaysinstruments.com
+92 344 4562520
How production, inspection and traceability are described
Manufacturing is managed in-house at the Sialkot facility. Heat treatment is completed by an external process provider.
For the applicable approved product scope, the company-level record also covers 100% visual and dimensional inspection and batch or lot traceability. Exact methods, criteria, records and product coverage remain subject to item review.
What should a buyer verify before approving a supplier?
The evidence should match the instrument family and order being assessed. Use this table to define the source pack you need.
| Area | Information or evidence to request |
|---|---|
| Facility and location | The approved company record covers the co-located Sialkot office and factory and the stated areas. Request any current, order-specific location evidence or factory-visit information required by your supplier-approval process. |
| Process map | A product-specific map covering material or component receipt through final packing, with the location of each step. |
| In-house and external work | Manufacturing is managed in-house at the Sialkot facility, while heat treatment is completed by an external process provider. Request the exact route for the product family under review. |
| Equipment and capability | The equipment or method used for the requested product family, plus any limits that affect the buyer's specification. |
| Materials | The material specification for the product family and the supporting records that can be supplied for the order. |
| Product development | The sample-development and approval stages, the responsible roles, and the record used to confirm approval. |
| Quality checkpoints | The approved company-level scope covers 100% visual and dimensional inspection for the applicable product scope. Request the applicable acceptance criteria and a representative record for the item under review. |
| Traceability | Batch or lot traceability is approved for the applicable scope. Request the identifiers and representative records available for the exact product and order. |
| Responsible roles | The roles responsible for production, quality review and buyer questions. |
| Packing and labelling | The proposed packing and labelling configuration for the order, including buyer-specific requirements. |
How to request manufacturing information or a quote
Send one request with the product and order context. If the request concerns manufacturing evidence rather than pricing, start the Message field with "Manufacturing information request" and list each item you need.
- The instrument family, product name or SKU
- Required patterns, sizes, finishes or other variants
- Expected quantity
- Buyer type and destination market
- OEM, branding, packing or labelling requirements
- The process information, records or documents you want to review
Base the decision on evidence for the actual order
Company-level manufacturing information does not confirm the specification, process route, inspection record, traceability record, conformity status, availability, price or delivery terms for every catalogue item. Request evidence for the exact products and order scope. Submission starts an enquiry; the item review or written quotation confirms what applies.
Request Manufacturing Information