01
Silver dermatome / skin-graft knife
Length, blade interface, material, handle and supplied components.
Surgical instruments · Catalogue and RFQ guide
Use this guide to shortlist catalogue records for skin-graft knives, manual dermatomes & replacement blades, compare the product attributes that need confirmation and prepare an itemised RFQ. Availability, specifications, materials, regulatory status, documentation, pricing, minimum quantities and lead time are confirmed only for the exact items and requested scope.
Guide updated . Catalogue records are references for enquiry preparation, not confirmation of availability or specifications.
01 / buyer details
Manufacturing base
Sialkot, Pakistan
Company history
Established 1996
OEM scope
Marking, labels and packaging
Documentation
Confirmed by product and market
Start with the way you buy
You do not need every catalogue number before contacting us. Choose the closest path, then refine the patterns, quantities and presentation with the product team.
Product architecture
Start with product families and selection logic. Exact models, materials and dimensions are confirmed against the current product record and approved sample.
01
Length, blade interface, material, handle and supplied components.
02
Adjustment range, mechanism, blade compatibility and fixation components.
03
Overall length, blade type, handle and compatible replacement blades.
04
Include only after current manufacture and exact variants are confirmed.
05
Dimensions, edge, packaging, compatibility and single-use/reusable status.
06
Model compatibility and supplied fasteners/components.
07
Blade guards, fitted cases and transport protection.
Faster starting points
These are quote-building starting points, not fixed clinical recommendations. Every component, piece count and case is confirmed before supply.
Turn an enquiry into a quoteable specification
Question 1 / 6
Make the range yours
Private label is more than a logo. The instrument list, physical specification, marking position, label content, packaging, case layout and inspection documents need one approved record.
01
Logo, article number, approved traceability text, placement and legibility are agreed against the physical instrument.
02
Protective sleeves, pouches, cases, cassettes, labels, inserts, barcodes and mixed-assortment packing are reviewed together.
03
Build a starter assortment, clear product tiers and a repeat-order SKU map around your target market.
04
Freeze the product list, sample, artwork, marking proof, packaging mock-up and packing list before production.
Show the checks that matter
The inspection method, approved sample and acceptance record are confirmed for the selected instrument and order—not implied by a badge wall.
Documentation and market support are confirmed against the legal manufacturer, product configuration and destination-market requirements before supply.
For United States and other regulated-market programmes, product classification, listing, labelling, UDI, reprocessing information and buyer responsibilities must be reviewed against the exact configuration. We do not use blanket “FDA approved” language for a general instrument range.
Prepare a document requestA controlled commercial process
Select product families, a bundle or share your current product list.
Agree patterns, sizes, materials, finishes, marking and packaging.
Review the agreed sample route and record any changes.
Confirm the quotation, artwork, packing list and document requirements.
Supply against the approved specification with the agreed inspection and export records.
Replace claims with evidence
These views belong in the product and sample evidence pack. We do not substitute AI-generated product or factory imagery.
Exploded system photograph
Blade/interface macro
Adjustment scale and mechanism
Compatibility chart by model
Fitted protective case
Dimensional inspection record
Curated catalogue
Use the catalogue record as a reference in your RFQ. Exact names, dimensions, availability and specifications remain subject to product-record review.
7 catalogue products
Catalogue product
Stainless Steel Silver Dermatome Skin Graft KnifeSKU: 54893Stainless Steel Silver Dermatome Skin Graft Knife (SKU 54893) is the reference to use when adding this catalogue record to an RFQ.
Catalogue product
Schink Skin Fixation PlateSKU: 54892Schink Skin Fixation Plate (SKU 54892) is the reference to use when adding this catalogue record to an RFQ.
Catalogue product
Schink Dermatome Replacement BladeSKU: 54891Schink Dermatome Replacement Blade (SKU 54891) is the reference to use when adding this catalogue record to an RFQ.
Catalogue product
Schink Dermatome - Precision Skin Graft KnifeSKU: 54890Schink Dermatome - Precision Skin Graft Knife (SKU 54890) is the reference to use when adding this catalogue record to an RFQ.
Catalogue product
Precision Dermatome BladeSKU: 54889Precision Dermatome Blade (SKU 54889) is the reference to use when adding this catalogue record to an RFQ.
Catalogue product
Watson Dermatome Skin Graft Knife - Precision Surgical InstrumentSKU: 54888Watson Dermatome Skin Graft Knife - Precision Surgical Instrument (SKU 54888) is the reference to use when adding this catalogue record to an RFQ.
Catalogue product
Professional Humby Dermatome - Precision Skin Graft KnifeSKU: 54887Professional Humby Dermatome - Precision Skin Graft Knife (SKU 54887) is the reference to use when adding this catalogue record to an RFQ.
Commercial questions
No. This page is a sourcing and enquiry guide. Confirm the exact product identity, specification, material, finish, status and applicable documents in writing for each selected catalogue record.
Yes, you can request a sample review. Sample availability, configuration, quantity, charges, freight responsibility, timing and the approval basis are confirmed in the written commercial response.
Yes. Dr. Jays International can review marking, branding, packaging, labels and private-label scope. Feasibility is confirmed for the exact item, artwork and requested presentation before an order is accepted.
Name the required record, product scope, destination, issuer, language and validity requirement in the RFQ. Document availability, applicability and permitted use are confirmed for the selected item and market.
No blanket product claim is made. Product classification, registration, listing, labelling, certificate scope and buyer responsibilities depend on the exact item, legal roles and destination market.
The written quotation confirms price, currency, quantity, sample terms, production scope and timing for the selected references, destination and requested work. No universal figure applies to every catalogue product.
Ready to define the range?
Start with a catalogue family, set direction or private-label brief. Selected references and questions remain requests until the item review and written quotation confirm the accepted scope.
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