Compliance
Our TİTCK and ÜTS registrations keep traceability on record from manufacturer to end user. Regulation is not paperwork we complete afterwards; it is the condition we start from.
Compliance and Documents
Quality is not a preference, it is an operational requirement.
We run legal compliance and product tracking through our registrations. Document status is published as it stands.
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ÜTS — Product Tracking System Registration
ActiveTraceability from manufacturer to end user is recorded through ÜTS. The document image is being prepared for publication.
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TİTCK Registration
ActiveOur registrations with the Turkish Medicines and Medical Devices Agency keep our distribution activity within the legal framework.
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ISO 13485 — Medical Device Quality Management System
In progressThe infrastructure required by the standard is in place; certification is under way. The certificate will be published here once issued.
Why it matters
Traceability is the first condition in choosing a supplier.
Which batch a medical device came from, the conditions it travelled in and who it was delivered to must all be on record. ÜTS makes that record mandatory, and we built our operation to produce it in full.
Consistency
More than 20 years in the field turned delivery quality into a standard that does not change by person or by city. A hospital in Ankara and a clinic in Hakkâri get the same service.
Care
We prioritise urgent shipments by knowing who is waiting for them. Packaging and temperature conditions for fragile items are tracked separately.
Write to us about your supply request.
Send your requirement list and we will confirm stock and availability within two business days.