English info@disposet.com +90 0312 256 26 06
EN ISO 13485
2016 Tıbbi cihaz kalite yönetim sistemi
CE sertifikası 93/42
eEC cihaz direktifi

Our Quality Policy

We look at each product
Each stage of our production is examined as part of our quality control system. Disposet manufactures according to internationally defined GMP Guidelines (Good Manufacturing Practices).

Our products are produced in modern production facilities under clean room conditions and according to approved production processes. These include in-process controls and traceability of all materials used. As a Disposet customer, you can always rely on the quality of our products.

EN ISO 13485: 2016 Medical Device Quality Management System
EN ISO 27716: 2007 GMP
CE certification 93/42 / eEC Device Directive

About. 4000 m2 closed area
Three independent Class 10,000 clean rooms; all about 600 m2
Class 100, Laminar Flow Cabinet
Verified Internal Sterilization Plant
Automatic packaging systems in every clean room
PE / PP Extruders and PU / PVC Extruders
Injection Systems; Both vertical and horizontal

R & D

Patented and Unique Design for atraumatic respiratory intubation system
Patented and Unique Design for a breathing circuit with adjustable internal volume.
Ear Drug Administration Tube design
New ring design for heart cover repair
Design of the clampless aortic surgery suture site system
Endoscopic Saphenous Vein lifting apparatus design