Frequently Asked Questions

• Biocompatibility testing
• Chemical testing
• Needle testing
• Packaging testing
• Visual testing
• Biological testing
• Mechanical testing

Each of our products that comply with CE conditions are subject to tests specified in the ISO 13485:2016 standard. These tests are repeated according to the intervals specified in the standard. Our tests are carried out by laboratories and accredited organizations approved by TÜRKAK or with the relevant competence.

• To select suppliers, dealers and authorized dealers to work with according to objective criteria,
• To fulfill our obligations on time,
• To select only qualified third parties with good references in terms of quality and honesty,
• To carefully protect the confidential information of the suppliers, dealers and authorized dealers we work with,
• To treat our suppliers, dealers and authorized dealers fairly and respectfully.

The body and pistons, which are syringe parts, are produced in plastic injection machines located in our sterile production area. Then, the printing strings are written on the body in screen printing machines. After the body, piston and seal are combined in the assembly machines, which is the next operation, they are packaged and boxed in packaging machines. The boxed products are subjected to the sterilization process in our ethylene oxide devices. Afterwards, the products are ready for shipment and are shipped to the relevant customer.

• We must ensure that the packaging is not torn or punctured and that the product has not come into contact with air,
• The lot number, production and expiration dates on it, and the content are complete.

Genject disposable syringes are mass produced in sterile environments and every stage of production is controlled, recorded and inspected. Syringe production is completely controlled by an automation system in accordance with GMP standards. It produces its products very carefully, not in a way that disregards human health but with full awareness of human health.

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