Industry Focus
Industries We Serve
Which certifications and test capabilities actually matter for your sector — and which are yours to hold.
Every industry asks an EMS a different first question. Medical device teams ask about quality-system certification and traceability. Industrial teams ask about temperature range, coating and part lifecycle. The underlying lines are the same — what changes is which evidence you need out of them.
What BELI holds, and what that does not cover
BELI's manufacturing is certified to ISO 9001:2015 (quality management), ISO 14001 (environmental management) and ISO 13485:2016 (medical device quality management). We are an IPC member, and our processes are RoHS- and REACH-compliant. Wire harnesses are built to IPC/WHMA-A-620 Class 2/3.
These are certifications of how BELI manufactures. They are not product approvals. A board built here does not inherit a medical device registration, a CE mark or a UL listing — those are granted to your finished product, by accredited bodies, against your documentation. What we provide is the manufacturing record and component traceability that supports your submission. The split is spelled out on each industry page below, and in more detail in our guide to CE, FCC and UL compliance for China-built PCBA.
The capabilities every sector draws on
Regardless of industry, the same confirmed capabilities are available: component sourcing through authorized distributors and original manufacturers with full traceability and original packaging, 100% visual plus X-ray sampling on incoming parts, AOI and X-ray on every order, ICT with 95% or better node coverage, flying probe, functional test, burn-in and environmental stress screening from −40 to +85 °C at 20–98% RH, a first-pass yield of 99.5% or better, and a test report with every shipment. Conformal coating, potting and box build are available as value-added options on the assembly line.
Industry Pages
Medical Device PCB Assembly (ISO 13485:2016)
ISO 13485:2016 certifies how BELI manufactures — not your device. This page sets out exactly which records you get and which parts of the regulatory file stay yours.
Read the medical device page →Industrial Automation PCBA Manufacturing
Control, drive and sensor electronics live with heat, vibration, condensation and ten-year lifecycles. Which of those pressures the confirmed capabilities actually address.
Read the industrial automation page →Working in a sector not listed here — telecommunications, security systems, consumer or instrumentation? The lines and the test capability are the same. What differs is the evidence package you need, so tell us what your sector requires and we will tell you plainly which parts we can evidence and which sit with you or an accredited lab.
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