Compliance & trust
We show our documents openly, with their status
We state separately which certificates have been obtained, which processes are in progress and what we have planned. Trust begins with not presenting an unfinished process as finished.
How to read the statuses
8 completed · 5 in progress · 1 planned
- Completed
The certificate or verification report has been obtained; its scope is as stated in the document.
- In progress
The application, contract or testing process is under way; the related marks and logos are not used until it is completed.
- Planned
On our roadmap; not yet started.
Management systems
Our quality, environmental, occupational health and safety, and customer satisfaction management has been certified by TÜV SÜD as an integrated system. The process for medical device quality management is in progress.
CompletedISO 9001
Quality management system
- Completed
ISO 14001
Environmental management system
- Completed
ISO 45001
Occupational health and safety management system
- Completed
ISO 10002
Customer satisfaction and complaints handling
- In progress
ISO 13485
Quality management system for medical devices
Environmental measurements and verifications
We measure our impact first. Life cycle, carbon footprint and water footprint studies were carried out using international ISO methods; the carbon footprint of one product has been verified by an independent body.
CompletedISO 14067
Product carbon footprint verification
Cradle-to-gate; applies only to the single product named in the document.
- Completed
ISO 14040/44
Life cycle assessment (LCA)
- Completed
ISO 14064-1
Corporate carbon footprint, 2025 base year
- Completed
ISO 14046
Water footprint
- Planned
ISO 14068-1
Climate target approach and measurable reduction plan
Product and regulatory conformity
Our processes relating to textile safety, personal protective equipment and medical device regulations are in progress.
- In progress
OEKO-TEX® STANDARD 100
Testing for harmful substances in textile products
- In progress
(EU) 2016/425
PPE Regulation (EU) 2016/425, Modules B and D
- Issuing body
- In progress
(EU) 2017/745
Medical Device Regulation (EU) 2017/745
- Issuing body
- In progress
EN 13795
Product testing for surgical drapes and gowns
Until these processes are completed, we do not present our products as “CE certified”, “MDR approved” or “certified”, and we do not use the related marks and logos.
Compliance & trust
Independent bodies we work with
We carry out our testing, certification and verification work with these bodies according to the scope of each project and document.
The listing of a body here does not mean that it has certified every one of our products; each result applies only to the product named in the report.
R&D support
TÜBİTAK TEYDEBR&D project supported under TÜBİTAK TEYDEB
KOSGEBKOSGEB Entrepreneur Business Development support
Countries we shipped products to in 2026
From our manufacturing facility in Türkiye, via the Mediterranean ports of İskenderun and Mersin.
- Italy
- Germany
- Netherlands
- United Kingdom
- Poland
- Switzerland
- Norway
- Iraq
An evidence card behind every claim
When we share a document or test result, we state the product, method, report number, date and scope of validity together. We do not extend one product's result to the entire brand family.
We prepare our environmental claims taking into account Directive (EU) 2024/825, which applies in the European Union from 27 September 2026.
Request a copy of a document or its scopeContact
Let's assess your project together
Share your need, your sector and your target timeline; we will direct you to the right team and specialist brand.