ÜTS Registration Services for Medical Devices
At QIS, we manage your company, document, and product registration processes in the Product Tracking System (ÜTS) with the support of our expert staff and experienced consultancy team.
If your company does not yet have ÜTS records for widely used products such as masks, gloves, disinfectants, or personal protective equipment (PPE), we can assist you with fast and fully compliant registration services.
Legal Obligation for ÜTS Registration
The sale of medical devices is regulated by law, and ÜTS registration is mandatory for every company involved in their production, import, or distribution.
ÜTS company registration is performed via MERSİS or VEDOP systems. If your company has both MERSİS and VEDOP numbers, you can manage all related transactions through the MERSİS platform.
Once your company registration is approved, the following documents are required for device documentation and product registration in the ÜTS system:
Required Documents for ÜTS Product Registration
- Authorized distributorship certificate
- EC (CE) certificates
- Company conformity declaration
- User manuals
- Quality management system certificate
- Domestic goods certificate (if applicable)
- Current product labels
- Sales package template uploads
Upon uploading these documents, your products will be registered in the ÜTS system. Our specialized consultants at QIS ensure all documents meet regulatory standards and your registration proceeds smoothly.
Additional Product Information Required for ÜTS
Below is the essential data that must be submitted during ÜTS product registration:
- Brand name
- Product number
- Quantity/units included
- Manufacturing and import details
- Product name
- Model or version
- Country of origin
- Regulatory class information
- Catalog or reference code
- Product label
- Branch and GMDN codes
- Original product images
- Product description
We guide you through every step to ensure full compliance and successful registration.
Why Choose QIS?
Thanks to our expertise in project management, QIS ensures a complete and accurate ÜTS registration process. When you choose to work with us, a dedicated consultant is assigned to your company to oversee and manage every phase of the registration.
We keep you informed at all stages—from document collection to final registration—ensuring that no step is missed and no time is wasted.
Start Your ÜTS Registration Now
If you are preparing to bring a product to the Turkish market, ÜTS registration is mandatory for both manufacturers and importers. With QIS by your side, your registration process will be:
- Fast
- Compliant
- Hassle-free
Our team ensures that every document and product detail, including barcodes and classifications, is accurately registered in the system.
Contact QIS for Expert ÜTS Registration Support
Don’t make a move without speaking to us. Contact QIS today to get a quote, receive free preliminary consultation, and ensure your company’s products are ready for market with full legal compliance.
Let QIS handle your ÜTS registration—so you can focus on your business growth.