Production
C-Tech products are manufactured, treated and packaged in our own production plants.
The following process are located in our premises:
- CNC machining
Numerically controlled Swiss lathes up to 10 axis and machining centers that allows to maintain tolerances of a few microns
Finishing with automatic tumblers
Automated tests with optical in-contact measuring machines with robotic anthropomorphic arm
- Regulatory and certification departments
Quality control in acceptance and batch release using periodically calibrated measuring instruments
- ISO class 6 clean rooms
Packaging of all sterile devices in an environment with controlled microparticle contamination
- Computer monitored packaging and tracing systems
After receipt and subsequent processing of the order, the shipping phase provides for complete traceability of the package to ensure that it reaches its destination in compliance with the agreed times
- Traceability of medical devices
Product traceability to check the supply chain from the batch of raw material to the delivery of the medical device in the sales configuration to the end customer
- Quality control departments
ISO 13485 certified company and CE marking of medical devices with the contribution of the body TÜV Rheinland. The quality system and the product are constantly monitored and subjected to annual inspections; this allows us to keep our quality system always up to date and aligned with the mandatory requirements. Being active in many non-EU markets, we are also active in the management of product certifications for these global markets
- CAD/CAM Planning
Through the use of 3D modeling software, drawings are created that are transformed into ISO machine language and transmitted to CNC machining centers
- CAD/CAM Milling Center
At the Milling Center, customized prosthetic elements are created by specialized dental technicians, using software and numerically controlled milling machines
- Guided Surgery planning
Using 3D software, a pre-surgical implant planning is performed first and then the surgical guide
- Guided Surgery stent production
Implant planning data is exported and imported into 3D software for virtual modeling and production of 3D models
- Product design and engineering department
Our specialized engineers are responsible for the realization of projects of all CE marked medical devices, in accordance with internal procedures and current ISO standards
With the sole exception of drill production, all our processes are in house and they are all governed by the highest level of production standards in the EU.
Independent and regular audits of all steps of production guarantee that all processes are following strict safety guidelines, ensuring at the same time they are up to date.
