Certificates & Compliance

Links to downloadable official documents are currently provided directly through the certificate images. Project-specific declarations for CoC, material declarations, CMRT, or audit support are also available.

gallery of Certificate

ISO 9001:2015 — Quality Management Systems

ISO 13485:2016 — Quality Management Systems for Medical Devices

ISO 14001:2015 — Environmental Management Systems

IECQ QC 080000:2017 — Hazardous Substance Process Management Systems

ISO 45001:2018 — Occupational Health and Safety Management Systems

IATF 16949:2016 — Automotive Quality Management Systems

UL Certificate — UL-related product or material documentation

RoHS Certification

REACH Certification

Note: No certificate number, expiry date, or audit report number is repeated in the card text; all those details remain within the linked official PDF.

What These Documents Mean for AVL Review

Faster Supplier Screening

These documents provide a streamlined procurement and quality review process by providing quick reference images of SUGA’s management systems and compliance documentation. Have you already downloaded the appropriate files and checked your company’s AVL checklist against them? If yes, you can submit a request for the documentation gap.

Clearer Audit File Preparation

By organizing system certificates, product compliance files, and declaration documents separately, you can reduce the time spent reviewing documents or exchanging emails after you send your audit file.

Project-Specific Document Path

If the audit requires a Certificate of Compliance, material declarations, Conflict Minerals Reporting Template (CMRT), or another document format not provided with the standard certificate PDFs, you will want to send SUGA the bill of materials (BOM), destination market, required document format, and audit checklist. This will allow SUGA to prepare the correct set of documents for you without requiring two rounds of clarification.

Compliance note: The certificates are issued to reflect the scope listed on each file as manufacturing-system or document support. Product regulatory approval, market authorization, and customer-specific compliance responsibility are the sole responsibility of the customer and are not implied by the certificates.

Request Documents

For CoC, material declarations, CMRT, or customer audit support, send your document list together with the confirmed BOM and project requirements.

Email: [email protected]

FAQ

Are SUGA’s certificate files available for supplier review?

Yes. Certificates are linked directly to their official PDF files. If you request a standard certificate copy by email, it can be sent within 1 business day.

Will SUGA’s ISO 13485 certificate be accepted by a medical electronics supplier audit?

Yes, the ISO 13485 certificate can support supplier qualification and medical electronics manufacturing auditing, but it is not the same as medical approval. The certificate is not a substitute for product approval, regulatory filing, CE marking, FDA clearance, or market authorization for a finished product.

Will I receive RoHS or REACH declarations with my shipment?

Yes. RoHS or REACH declarations can be available for orders that require them. See the Project-Specific Document Path section above.

Is there any other information necessary for me to provide to SUGA in order to issue project-specific compliance documentation?

SUGA requires the confirmed BOM, product category, destination market, document type, and customer audit checklist. Supplier-level information may also be requested for CMRT or material declarations.

Can SUGA assist me with an urgent AVL or customer audit request?

Yes. Start with the certificate files above, and provide SUGA with a completed audit checklist and missing document list. SUGA can separate standard certificate copies from CoCs, material declarations, CMRT, or factory audit support requests so the urgent AVL review does not have to wait for responses about unrelated documents.