Global Reach. Local Support.
We carry a wide range of materials from the world’s top medical resin suppliers, including USP Class VI and ISO 10993 certified biocompatible resins with full FDA Master File support. Our portfolio approach offers the most expansive selection of medical resin materials in the industry, balancing performance, cost, reliability, materials, and shelf life with your application’s specific needs.
Our regionally-based technical engineers are true materials and processing experts who are organized to function as an extension of your design and engineering value chain. Our goal is to deliver the trusted total solutions that meet your exacting specifications and medical plastic needs. We also offer a wide variety of technical services in our A2LA certified lab are available at little or no charge to support your project.
From concept to production, we’ll work with you through any stage of your development process to help you overcome engineering and design challenges, realize your project goals and achieve a competitive edge in your market. Entec has decades of medical application development experience and a portfolio of medical resins to address your application needs.
The Ravago Group, parent company to Entec Polymers, is one of the earliest members and strategic advisor to the Healthcare Plastics Recycling Council (HPRC), a private, technical consortium of industry peers across healthcare, recycling and waste management industries to improve the recyclability of plastic products and packaging within healthcare.
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Looking for materials for your application? Our team of experts can help you select the best resin for your project.
Whether used for a single procedure or reprocessed, today’s certified medical plastics enable product engineers to meet strict performance and reliability criteria in a wide variety of surgical instrument applications across all risk classifications. Entec can help simplify material options to minimize surface interactions, survive sterilization processes and meet strict end-use design requirements.
Delivering clinical performance and patient safety at the lowest possible cost is the very definition of why single use disposable devices are used in virtually all clinical procedures. Designing these products starts by understanding user requirements and then balancing performance, cost, reliability, materials, and shelf life.
From simple syringe components to sophisticated and automatic injection devices, the goal of every drug delivery device is simple: Accurately delivering the exact amount of therapeutic drug needed every single time. While the concept is simple, achieving this goal using a variety of different medical materials can be complex without the right experienced partner.
Medical packaging can also be referred to as barrier packaging and is a critical component to patient safety and effective treatment. Packaging provides a barrier against moisture, oxygen and light while maintaining a product’s sterility in many cases. In the case of APIs, effective barrier packaging guarantees efficacy and shelf life claims.
Whether used in a clinical setting or in the home, purchased or rented, medical companies expect their products to provide long-lasting value, high-performance and exceptional quality. From simple braces to multi-million dollar machines, a wide variety of plastics play an integral role to the long-term clinical performance of these applications.
Most of today’s high-performance medical fabrics are SMS nonwovens produced using plastics, balancing performance and cost with strength, flexibility, air permeability and rated barrier requirements.
Low cost but high-quality plastics free of contamination and capable of being resterilized is the benchmark of labware plastics used in many testing regimens. Exceptional optical properties and high heat resistance are two other properties which allow plastics to replacement of other more expensive materials such as glass and quartz.
Although this category has existed since 1938 with the invention of the first hearing aid, technological advancements have revitalized the convergence between wearables and medical products. The product’s reliability, expected life cycle, resistance to body fluids and haptics must all be carefully considered to produce a device which meets stringent safety and accuracy standards.
Reducing the incidence of Healthcare Associated Infections (HAI) by sterilizing medical equipment with today’s caustic chemical disinfectants has created a need to rethink this critical material selection. These chemical disinfectants attack molded-in stresses, causing cracking, crazing, loss of impact strength and eventually premature device failures. Available exclusively through Entec, Ravago’s MedArmor line of resins have been specifically engineered to resist this new generation of chemical disinfectants with proven efficacy.Download Product Guide