Cedic S.r.l.
At Cedic we offer solutions for living. Our diverse product portfolio, specialising in fluid delivery, is designed with the main objective of improving the patient’s quality of life. That is why we continually invest in our people and facilities to remain at the forefront of innovation and responsive to market needs. Our partners can rely on effective solutions and consistent quality coming from our three dedicated manufacturing facilities in northern Italy. We have over 50 years of experience in the medical devices industry, boasting the latest technology, cutting-edge automation and active collaboration with AAMI and ISO organisations in standards development. In an ever changing healthcare market, it is no wonder why we are a preferred supplier to major industry players.
Company details
Find locations served, office locations
- Business Type:
- Manufacturer
- Industry Type:
- Medical Equipment
- Market Focus:
- Globally (various continents)
This company also provides solutions for other industrial applications.
Please, visit the following links for more info:
Welcome
AT CEDIC WE OFFER SOLUTIONS FOR LIVING.
Headquartered in Milan, Italy, our capabilities range from design engineering through to finished device manufacturing.
We specialise in fluid delivery and our varied product portfolio, consisting of single components to sterile OEM devices, is distributed in over 40 countries.
We strive to be a global innovation leader in the field of Medical Devices focusing on Enteral & Perfusion.
About Us
At the forefront of innovation
At Cedic we offer solutions for living. Our diverse product portfolio, specialising in fluid delivery, is designed with the main objective of improving the patient’s quality of life. That is why we continually invest in our people and facilities to remain at the forefront of innovation and responsive to market needs.
Our partners can rely on effective solutions and consistent quality coming from our three dedicated manufacturing facilities in northern Italy.
50 years of experience
We have over 50 years of experience in the medical devices industry, boasting the latest technology, cutting-edge automation and active collaboration with AAMI and ISO organisations in standards development.
In an ever changing healthcare market, it is no wonder why we are a preferred supplier to major industry players.
End-To-End Medical Device Manufacturing
Concept Phase
Concept ideation & project scheduling
Development
Prototype development & design freeze
Testing
Design verification & validation
Industrialisation
Injection moulding & assembly process validation according to client needs
Production
Production ramp up to anticipate market demand
Distribution
Worldwide supply chain network
INNOVATION
We have spent the last 50 years developing our internal R&D and Project Management capabilities of finished products and components which now comprise:
- Rapid prototyping via 3D Modeling & 3D Printing
- Technical feasibility & assembly technology evaluation
- Finite Element Analysis
- Verification and Validation (V&V) in-house testing
- Moulding process definition, optimisation & qualification
- Assembly process validation (IQ, OQ, PQ)
- Statistical analysis, Design for Six Sigma approach
- Knowledge of applicable ISO standards
Our facilities have been awarded a AAMI (Association for the Advancement of Medical Instrumentation) Standards Extraordinary Achievement Award for design and analysis efforts which exceed the ISO 80369 series of standard.
Ensuring only the best materials are sourced and sustainable packaging is used, our procurement department has evolved to be highly specialised in procuring for the medical devices industry. Clients can rest assured knowing that we utilise controlled sources from a long-standing network of credible suppliers.
Our procurement colleagues also work closely with the many technical experts within Cedic to support specific project needs and foster product innovation with the necessary equipment and machinery.
Our Quality Management System (QMS) complies with ISO 13485 standard and is MDSAP certified for Australia, Brazil, Canada, the United States and Japan.
Patient safety is guaranteed through product CE certifications, FDA clearance and compliance with the applicable ISO standards , such as ISO 14971 for conducting Risk Management. All this is strengthened by our robust QMS involving rigorous control procedures throughout the entire product lifecycle.
Our automated assembly lines boast 100% in-process quality controls and our manually assembly lines carry out controls at every stage of production. Over and above these in process controls, incoming inspection and final inspection prior to product release are routinely performed by qualified personnel.
We mould over 500 million components annually encompassing various areas of care with extensive capabilities including:
- ENFit® transition adapters
- Screw caps
- Spikes
- Administration set components
- Tube feeding connectors
- Enteral feeding caps
- Luer-lock connections
Our clean rooms are ISO class 8 certified where we can work with a variety of raw materials including, but not limited to ABS, PP, LDPE, TRITAN, HDPE, PVC, PS, EVA and TPE.
Our sophisticated automated assembly lines ensure speed to market, consistent high product quality and cost effectiveness complete with 100% in-process quality control. While our manual assembly lines allow us to guarantee a high level of flexibility to accommodate a wide range of specific customer needs.
These lines are set up to produce diverse range of sub-assembled products and finished medical devices.
In-house customised packaging and printing capabilities with various print and design options to suit our clients’ needs. Our labelling operation is also equipped to automatically blister products of various shapes and sizes.
What’s more, we are qualified to check the validity of labels and to validate EO sterilisation for our clients’ own products upon request.
We have the internal resources and expertise to file and maintain product registrations worldwide including FDA clearance and CE markings.
Our experienced regulatory team is on hand to support our customers through the registration process from start to finish; from filing the application to labelling and proofing and are across the latest updates and requirements.
We have over 8’500m2 of warehouse space and ship to over 40 counties across the globe.
Our supply chain department is well-established and connected with major freight forwarders around the world. We place a strong emphasis on reliability and are committed to delivering in full and on time.
To accommodate desired lead times, freight terms and customs requirements, we are proficient in arranging a variety of shipping methods including truck, sea, and air freight.