Resources
Documentation for procurement, QA, and OEM teams.
This page collects the documents AJ Brothers Enterprises buyers ask for most often during qualification, regulatory submission, and sample-evaluation phases. Most resources are NDA-gated and sent on request within one business day.
Catalog and product specs
- Master catalog (PDF) — every SKU we make, with model number, dimensions, material, MOQ, lead time, and reference photos. Send to sales@ajbrothersent.com to receive the latest version.
- Per-product spec sheets — drawing, dimensional tolerances, finish, sterilisation compatibility. Linked from each catalog entry.
- Custom drawings + tolerance docs (NDA) — for OEM partners working from a buyer-supplied spec. See OEM & private label for the engagement workflow.
Quality and regulatory
- ISO 13485:2016 certificate scan — current, with registrar verification link. Request from qc@ajbrothersent.com.
- CE Declaration of Conformity — per affected product family, EU MDR 2017/745 compliant.
- EU MDR / EUDAMED registration data — Basic UDI-DI and UDI-DI lists per product family.
- FDA 510(k) clearance summaries — for affected SKUs. Most general dental and surgical instruments are 510(k)-exempt; specialty SKUs requiring 510(k) are documented per line.
- Material certificates — per lot. Stainless 420 / 410 / tungsten-carbide / titanium origin traceability available.
- Latest audit reports (NDA) — annual surveillance audit, re-certification audit. NDA before disclosure.
- See the quality framework for the full document chain.
OEM and distributor packs
- Mutual NDA template — we send within one business day on first OEM contact.
- OEM sample kit order form — three samples per SKU, your spec, your finish, your marking. Sample-kit fee credited against first production order.
- Distributor application + tier matrix — three-tier partnership model. See distributors.
- Co-branded marketing assets — product photography, brochures, and regulatory packs in your brand for Tier 2+ partners.
Audit-prep documents
- “What to expect on a Sialkot audit” (PDF) — agenda template, factory-floor route, document-review checklist. Sent ahead of every scheduled visit.
- Sample lot traceability pack — we will pick any lot we have ever shipped and assemble the full document chain (QC certificate, dimensional check sheet, polish sign-off, carton lot card). Use this to dry-run your audit before flying in.
- Book a factory audit — two weeks notice.
How to request
Email the team contact above for each document, or use the quote form and add “documentation request” in the message field. We reply within one business day, Monday to Saturday, Sialkot office hours (09:00–18:00 PKT, UTC+5). NDA is sent within the same window for any document marked NDA-gated above.