ISO 9001:2015
SupportsA certified quality-management framework for procedures, records and corrective action.
Verify nextThe control plan, inspection records and FAT criteria for the selected machine. ISO alone does not prove process capability.
Procurement + quality + EHS + engineering
Request documents by review question, not by logo.
The homepage identifies CKD's certificates. This page separates what each record supports, what it does not prove, and which project-specific file should follow.
ProcurementIdentity, quality system and supplier status.
QualityControl records, FAT and acceptance evidence.
EHSElectrical, laser and machine-safety scope.
EngineeringConfiguration, utilities, interfaces and process result.
Role-based review matrix
Give each reviewer the file that answers their question.
| Reviewer | Start with | Question answered | Project-specific follow-up |
|---|---|---|---|
| Procurement | Company credentials, ISO 9001 and intellectual-property management record. | Is the supplier identity and management system traceable? | Commercial scope, warranty, delivery schedule and supplier questionnaire. |
| Quality | ISO record plus the factory control and measurement plan. | How are critical characteristics measured and released? | FAT checklist, sample results, repeatability data and open-action closure. |
| EHS | Applicable CE reference and the standards listed for the selected equipment scope. | Which electrical, EMC and laser-safety requirements are referenced? | Declaration/certificate for the exact model, safety circuit, interlock list and site EHS checklist. |
| Engineering | Model specification, layout, utilities and interface description. | Can the selected machine meet the actual application and line conditions? | Sample plan, process window, CAD/interface files and agreed acceptance criteria. |
What each record supports
Certificates establish scope; project evidence proves the machine.
GB/T 29490-2013
SupportsA management framework for intellectual-property records linked to machine, software and process development.
Verify nextWhich software, process or patent is relevant to the selected application. The certificate is not a performance test.
CE Directive 2014/35/EU
SupportsAn electrical-safety reference in the supplied certificate material, together with EMC and laser-related standards.
Verify nextThe exact model, certificate/declaration scope and applicable technical file. Do not assume one record covers every configuration.
100+ patents
SupportsA traceable ownership base across brittle-material processing, laser deflashing and automation.
Verify nextThe relevant patent or software record and the actual sample result. Patent count does not replace application validation.
Document pack by project stage
Request the pack in three controlled releases.
1. Supplier screening
Company identity, ISO 9001, intellectual-property management record, relevant corporate qualifications and the initial product specification.
2. Process validation
Sample definition, process window, result format, applicable safety reference, layout, utilities and line-interface description.
3. FAT and acceptance
Model-specific certificate/declaration scope, FAT checklist, measurement results, sample record, manuals, training scope, packing list and open-action closure.
Standards referenced in source material
Confirm applicability against the exact machine.
The supplied CKD certificate summary references the following standards. Their applicability, edition and configuration scope must be confirmed in the project document pack.
Certificate reference list
- EN 60825-1:2014/A11:2021
- EN IEC 55014-1:2021
- EN IEC 55014-2:2021
- EN IEC 61000-3-2:2019+A1:2021
- EN 61000-3-3:2013+A2:2021
This list is a source-material index, not a blanket declaration of conformity for every CKD model.
Name the reviewer, model and required evidence.
CKD can confirm which records apply to the selected configuration and which project-specific files are prepared during sample validation, FAT and delivery.