Certifications
CERTIFICATIONS & APPROVALS
High standards & optimal solutions
Duelco has achieved several significant certifications, including ISO 9001, AAA and MDD/MDR.
These seal of approvals confirm that we continuously strive to maintain the highest standards of quality, safety and performance in our products, solutions and processes.
As a customer, you can have full confidence that the solution you choose meets strict industry requirements.
ISO 9001:2015
Certified management system
Duelco is certified with ISO 9001:2015 for our management system in the industry 'sales of solutions for electrical and automation equipment'. Achieving ISO certification is a long process of proving that the management system meets all the requirements for standardization and quality assurance set by ISO (International Organization for Standardization).
On the other hand, ISO certification is a seal of approval that creates security and trust both externally and internally.
ISO is an independent, non-governmental international organization that develops standards to ensure the quality, safety and efficiency of products, services and systems.
AAA
Highest credit rating builds trust
A AAA credit rating is considered a seal of approval and a strong indicator of a company's financial stability and reliability. The certificate also signals Duelco's commitment to sound financial practices.
The credit rating provides great credibility in the market and strengthens the trust of our business partners and customers.
The AAA rating is awarded by independent credit rating agencies.
MDR [in process, pending]
Regulations for medical devices
MDR stands for 'Medical Device Regulation' and is a new set of rules regulating the production and distribution of medical devices in Europe. It was introduced to ensure that EU legislation keeps pace with scientific and technological developments.
The MDR, which replaced the MDD from May 2021, raises quality and safety requirements and introduces stricter controls on high-risk products, more detailed marketing surveillance and greater transparency for consumers.
MDR is mandatory for companies that want to manufacture and sell medical devices in Europe.
MDD
Securing medical devices in the EU
MDD stands for 'Medical Device Directive' and is the legal framework for the production and distribution of medical devices in Europe before May 2021. It was introduced to ensure that EU legislation keeps pace with scientific and technological developments and that safety is paramount.
The regulations include provisions for the design, manufacture, approval, labeling and clinical evaluation of medical devices.
The new rules, MDR, replaced the MDD rules in May 2021.
Need more information?
Add to your download list or download instantly.
