Procurement
Uses product sheets, packaging details, sample information, and quotation details to compare suppliers.
QA and product documents
Request the files procurement and QA teams need before approval.
Ask for product sheets, IFU, Declaration of Conformity, packaging, labeling, sterilization, distributor, and market-entry files with the product family attached.
The RFQ page will open with Documents selected and this file request in the remarks field.
Available document requests
Ask for the compliance files that match your review stage.
Quality system
ISO / CE certificate details
Ask which ISO 13485, CE, MDR, or company-level QA files can be shared for the product family and market.
Registration
IFU, DoC, and technical file
Request Instructions for Use, Declaration of Conformity, product sheets, technical file, dossier, or FDA registration review details where applicable.
Tender / logistics
Packaging and sterilization files
Request packaging specifications, labeling files, sterilization information, carton details, FSC details, or tender-support documents.
Helpful details
A few details help us send the right files faster.
Select your productChoose a category, ViaSurg SKU, current model, catalog page, tender line, or product photo.
Choose required documentsIFU, DoC, CE/ISO certificate details, product sheet, packaging, labeling, sterilization, FSC, or technical file details.
Specify your marketTell us the country or region, your team’s role, and whether this is for tender, registration, distributor onboarding, or QA review.
Who uses these files
Document support for each buying team.
Distributor
Uses market entry documents, labels, product sheets, and FSC details for hospital or tender conversations.
QA / RA
Uses IFUs, DoC, technical file details, certificate details, and destination-market notes for compliance review.
Related paths
Connect document needs with the product family and buying stage.
Keep document requests connected to product family, cross-reference details, comparison parameters, or the RFQ page.
Document FAQ
Common document request questions.
Can I request CE, ISO 13485, IFU, DoC, or technical file details before a quote?
Yes. Send the product family, destination market, your team’s role, and file type your QA or distributor team needs.
Can you support FDA or 510(k) document questions?
Send the intended market, product family, and review purpose. ViaSurg can respond with the appropriate registration or document review process where applicable.
What if I only have a current item or tender line?
Choose cross-reference review and include the document need in the same request.
Compliance support
Give QA/RA enough details for a useful first reply.
The document request collects product, market, role, and required document details so the first response can be specific.
Select your productFamily, product page, SKU, current model, tender line, or cross-reference details.
Specify your marketDestination market, distributor role, QA/RA need, or labeling details.
Clarify the file purposeTell us whether the files support tender review, distributor onboarding, registration questions, packaging checks, or QA approval.
Document request
Tell ViaSurg which files your QA, RA, or distributor team needs.
Share product family, target market, your team’s role, and required file type so the response can be specific.
QuoteTarget quantity, purchasing stage, and destination market.DocumentsProduct sheets, packaging files, labeling notes, and QA documents.SamplesTrial quantity, product family, packaging expectation, and deadline.Packaging / labelingArtwork, sterile-pack format, and market language.Cross-reference reviewCurrent brand, model number, catalog page, tender line, or product photo.OEM projectDrawing, sample, product family, volume target, or packaging brief.