Healthcare
Mold making and injection molding in a hygienic production environment and cleanrooms. Clean silicone and multi-component parts for the healthcare industry.
Our Expertise:
ISO 13485
Cleanroom Production
ISO 13485 – Manufacturing with a Hygiene Plan
From concept to finished product—at RICO, you'll find decades of expertise in the medical industry.
Since the company was founded in 1994, we have been manufacturingtools for the medical technology industry, and since 2009, we have also been producingsilicone parts for mass productionthat meet specific product requirements (regulatory and standards-based)inour own cleanrooms.
RICO is certified to EN ISO 13485:2016. This underscores our quality philosophy and our focus on the medical technology industry. We meet high hygiene standards throughout the entire production process, thereby offering reliable solutions for sensitive applications.
The RICO GROUP has many years of experience in the cleanroom manufacturing Class 7 and 8 for the medical technology industry.
A trusting and reliable partnership is important to us. We handle your projects with the utmost care and confidentiality, and we see ourselves as a stable partner for your risk management. We advise you on material selection, build prototypes, and provide you with comprehensive solutions—right down to shelf-ready packaging—for your product.
Advantages of Silicone in Medical Technology:
- Allergen-Free
- Biocompatibility
- High-temperatureresistanceandlow-temperature flexibility
- Goodresistanceto alcohol, polar solvents, and weak acids
- Optical siliconesforcrystal-clear applications
Healthcare Production Examples
- Componentsfordisplays and control elements, optical devices, pressure gauges, surgical procedures (e.g., sleeves), and syringe components
- Valves: Duckbill valves, flow valves, needle-free valves, …
- Microcomponents
- Implants
- Visible and functional parts: membranes, sealing elements, caps, push buttons, masks, dampers, O-rings, …
- Custom Solutions
RICO Cleanroom for High-Precision LSR Manufacturing
- Cleanroom production in accordance with ISO class standards for high-performance LSR components
- Contamination-Free Manufacturing Through Controlled Environmental Conditions
- Integrated Automation & Handling Solutions for Stable Mass Production Processes
- Maximum process reliability and traceability
Optimized for medical, automotive, and electronics applications - Efficient Operations Through Coordinated Material, Machinery, and Personnel Processes
What does EN ISO 13485:2016 certification mean?
The ISO 13485 standard is a certification for the medical technology industry. It specifies the requirements for a comprehensive quality management system for the design and manufacture of medical devices. The overarching goal of the ISO 13485 standard is to ensure product safety and effectiveness with regard to the design, manufacture, and marketing of medical devices. Security measures for the storage of patient-related data are also part of ISO 13485.
We look forward to hearing from you!
Please use our contact form or contact our sales team directly.
You can reach our internal sales team at +43 7242 76460 0215 or by email at sales@rico.at
Healthcare Article
Our Industries
Our diverse mix of industries and the fact that we handle both tooling and injection molding production for our customers make us a particularly reliable business partner with comprehensive industry expertise.
