Advances in Materials Characterization of Medical Device Webinar
In this webinar we introduce EAG Laboratories advances in Materials and Surfaces Characterization of Medical Devices
Are You Prepared for the New EU Medical Device Regulation Webinar?
In this webinar we introduce how a 3rd Party Analytical Lab Can Help Support Your Company’s Compliance with EU’s MDR
Ask the Expert: Elemental Analysis with ICP
June 27, 2024
During this live Ask the Expert event, we will answer pre-submitted questions from our audience regarding Elemental Analysis with Inductively Coupled Plasma (ICP-OES, ICP-MS, LA-ICP-MS). These techniques provide full survey major, minor, trace element analysis, and purity certification for up to 69 measurable elements.
Ask the Expert: Is Your Wearable Device Safe?
In vitro biocompatibility testing is a powerful tool in the risk assessment of wearable devices. View our webinar to learn more!
Assessing Nickel Leaching on Cardiovascular Stents
EAG evaluate corrosion and leaching of nickel-rich implanted medical devices including nitinol, stainless steel and MP35N.
Assessment of Nickel Exposure Risk of Intravascular Stents and Delivery Systems
Nickel biocompatibility assessments of intravascular stents from EAG includes evaluating corrosion, surfaces and nickel ion release testing.
BioInterface 2024
October 2-4, 2024
Eurofins EAG Laboratories will present at the 34th Annual BioInterface Workshop & Symposium.
Biomedical Morphology
Biomedical Morphology and Microstructure through imaging analysis – characterizing crystallographic phase and producing elemental maps.
Biomedical Surface Analysis
Biomedical surface analysis looks at properties critical to medical and pharmaceutical products, and offer answers to difficult problems.
Catheter and Balloon Analysis
Catheter and balloon analysis for medical device development support includes deformulation, contaminant identification and failure analysis.
Characterization of Bioceramics for Surgical Implants Webinar
In this webinar we introduce Characterization of Bioceramics for Surgical Implants using analytical tools for full qualification
Characterization of Bioceramics for Surgical Implants: Part I – Precursor Qualification
This paper will demonstrate how analytical tools can be used for the quality control of hydroxyapatite and β-tricalcium phosphate powders
Characterization of materials used in stents
Stents characterization from EAG includes nitinol, stainless steel and MP35N. Experiences with fatigue resistance and hydrogen embrittlement.
Chemical Compatibility of Polymers in Medical Devices Webinar
In this webinar we introduce Chemical Compatibility of Polymers in Medical Devices and prevent material problems in the field
Contact Lenses: Understanding Surface Chemistry Critical to Optimizing Design
EAG Laboratories helps you understand contact lenses surface chemistry, critical to optimizing design and engineering optimal performance.
Corrosion Resistance Study of Electropolished Medical Devices
Medical device corrosion resistance optimized by using Auger depth profile & oxide layer thickness for device surface characterization.
Corrosion Testing for Medical Devices
This webinar covers FDA regulation of medical devices, the most commonly used test standards, and custom testing at Eurofins EAG Laboratories.
Cracking of Molded Components
An injection molded component in a consumer product was found to have an increased failure rate over a three-month period.
Curing Issues with Silicone Adhesive
A client requested assistance to investigate a recurrent issue with the curing failure of a silicone adhesive joint between metal components.
Delamination of Food Packaging
A client wanted to investigate the delamination of food packaging multilayer laminate. Roll stock did not meet seal strength specification.
Design an Effective Chemical Characterization Study for Your Device
May 15, 2024
Check out our online symposium presented by EAG Laboratories and Exponent!
Driving medical device innovation and development
EAG Laboratories offer comprehensive testing for materials, electronics and drugs for medical offerings
EAG Expands Medical Device Testing Services
6th May 2021
EAG Laboratories has expanded its medical device testing capabilities with a new laboratory located in St. Louis, Mo.
EAG Recognized as a Top 10 Corrosion Services Provider
13th December 2022
Manufacturing Technology Insights recently named EAG Laboratories a Top 10 Corrosion Services Provider. The publication featured an interview with Dana Medlin, our Vice President of Metallurgical Engineering.
EAG Recognized as Top Corrosion Services Provider for Second Year In a Row
August 28, 2023
Manufacturing Technology Insights named Eurofins EAG Laboratories a Top 10 Corrosion Services Provider for the second year in a row.
EAG Secures DLA MIL-STD 883 TM 1018 Suitability
17th November 2022
EAG has been approved as a suitable commercial laboratory to provide MIL-STD 883/750 Test Method 1018 Internal Water Vapor Content Testing for hermetically sealed electronic devices.
EAG Successfully Completes ISO 17025 Accreditation and Expands Scope to RGA Testing
8th June 2023
Now, with RGA included in the scope of ISO 17025, RGA testing at EAG is a premium choice to perform gas analysis.
Effects of Surface Roughness
The roughness of a surface and how it interacts with surrounding materials and elements can have a significant impact on material technology and its functionality.
Elemental Composition using XRF
XRF is a non-destructive technique that is used to quantify the elemental composition of materials.
Environmental Stress Cracking of a Polycarbonate Part
A company was investigating environmental stress cracking of polycarbonate components used in a conveyor device that was sanitized.
Essentials of Particulate Testing: USP <788> and AAMI TIR42
Essentials of Particulate Testing: USP <788> and AAMI TIR42 While there are many standards available for particulate testing, USP <788> and AAMI TIR42 are the
Evaluating the Cleanliness of Medical Devices
Eurofins EAG has a wide array of analytical techniques to verify the cleanliness of medical devices. We’ve helped our customers evaluate the cleanliness of their products using techniques including NVR analysis, often in combination with FTIR, XPS and TOF-SIMS.
Evolved Gas Analysis for Material Outgassing Characterization
All materials have trapped gasses inside. Learn how EAG utilizes Evolved Gas Analysis to analyze what gasses are being released.
Excluded Compound Testing
Exclusion Testing for Material Compliance Regulations of Medical Device Components has multiple regulating bodies.
Extractable and Leachable Database Building for High Confidence Identification by Liquid Chromatography-Mass Spectrometry
Through database building, EAG provides higher-quality chemical characterization reports with reduced turnaround times to support medical device biocompatibility programs.
Extractables & Leachables West 2024
November 13-14, 2024
Eurofins EAG Laboratories will present at Extractables & Leachables West 2024.
Extraction Expertise for Medical Device Chemical Characterization
EAG offers advanced expertise and a risk-based approach for medical device extractable study design and execution, including the latest FDA expectations.
Failure Analysis of Medical Device Electronics
As medical devices become more complex, there are many more opportunities for things to go awry. Identifying, diagnosing, and remedying failures becomes dramatically more challenging. We can help.
For Medical Device Testing, Every Variable is Important
The analytical evaluation threshold (AET), an important part of the extractables and leachables testing in these studies, needs to be calculated for each instrumental technique.
Frequently Asked Questions About In Vitro Irritation and Cytotoxicity Testing
Biocompatibility assessments are a battery of tests performed to evaluate a product, medical device, or other material for the risk of biological hazards.
From Certifications To Customer Audits, Quality Matters
EAG Laboratories pursues quality in all aspects of our work for customers. ISO certifications and ongoing audits serves many market sectors.
FTIR and Raman – Composition and Contamination Analysis
FTIR and Raman are spectroscopy techniques that provide molecular information from various types of materials.
GMP, GLP or ISO 17025: How Do These Apply to Outsourced Analytical Testing?
Medical device regulations are not entirely clear, EAG shows the decision process for contract analytical laboratories to support development.
Implementing Extractables and Leachables into Quality Control Testing Programs
E&L methods pose challenges as they transition from R&D environment to routine QC testing. Understanding these challenges will help you avoid costly delays.
In Vitro Diagnostics Testing
In Vitro Diagnostics test and system development support from the materials sciences experts at EAG Laboratories, contact us today!
Incompatible Contaminant in Tubing
A device manufacturer observed defects in a lot of thermoplastic tubing. The tubing exhibited signs chemical attack or exposure to heating.
Is my surface clean? Effects of Surface Cleanliness
Surface cleanliness is critical in how a material or a layer on a product interacts with other surfaces, which in turn can affect its functionality.
Laboratory and Testing Support for Companies Manufacturing Medical Supplies to Fight COVID-19 (Coronavirus)
Respiratory protection testing, cleaning compatibility, sanitizing liquids and wipes, supply chain and manufacturing quality, failure analysis
Master the Toxicological Risk Assessment of Your Device with Better Chemistry
December 12, 2023
Check out our online symposium presented by EAG Laboratories and Gradient!
MD&M West 2025
February 4-6, 2025
Eurofins EAG Laboratories will exhibit and present at MD&M West in Anaheim. Dr. Philip Ferko, Senior Scientist with EAG, will present in the MD&M West Center Stage at 12pm on February 4.
MEDevice Boston 2024
September 25-26, 2024
Eurofins EAG Laboratories will exhibit and co=present with Gradient at MEDevice Boston 2024.
Medical Device & Diagnostics for BIOMEDevice
Drive productivity while keeping pace with evolving regulations
Medical Device Electronics: Improving Reliability with Auger Electron Spectroscopy
Auger Electron Spectroscopy applied to electronic circuitry problems involving the integrity of wire or ball bonding to metallic bond pads.
Medical Device Testing Brochure
Ensuring medical devices are safe, compliant and effective
Medical Devices and Diagnostics
Device concept and medical device researchers need materials answers quickly so the can proceed with device development. Ask EAG!
Molded In Stresses
Cracks were observed in transparent thermoformed plastic packaging during visual quality checks. Failures occured in specific material lots.
North American Biocompatibility Summit (NABS) 2024
September 11, 2024
Eurofins EAG Laboratories is the presenting sponsor for the North American Biocompatibility Summit (NABS) at Quincy Hall in Minneapolis, Minnesota.
Off-Odor Memory Foam
Analytical testing to support changes in raw materials and processing conditions used in manufacturing memory foam, as well as odor
Orthopedic Implants
Orthopedic implants composed of metallurgical alloys, plastics and critical surface chemistries require characterization
Part 18: Chemical Characterization of Materials
Part 18: Chemical characterization of materials, part of ISO 10993 pertains to evaluating biocompatibility and safety of medical devices.
Polymer Case Study: Blistering Paint
Blisters were observed in paint applied to steel plates that had undergone treatment with a corrosion inhibitor. An investigation was performed to determine if there was evidence of contamination on the inside of the blister.
Principles and Strengths of In Vitro Testing
In Vitro testing uses cell-based biological models instead of animals or humans.
Residual Gas Analysis for Hermetically Sealed Devices
To be hermetically sealed essentially means to be airtight so that nothing can come in or get out (i.e., gas, moisture, liquid, etc.).
Residual Solvents in Medical Devices
Detecting Levels of residual solvent concentrations in medical devices with Dynamic headspace Gas Chromatography-Mass Spectromety (GC-MS)
Restricted Substances Impact Everyday Products
As the list of restricted substances grows, testing demands customized methods to identify issues early. This is a complex issue that requires a strategic approach.
Root Cause Determination of Adhesion Failure in Medical Device Packaging
XPS and TOF-SIMS to solve adhesive failure of a polyethylene-ethylene acrylic acid (co-polymer) heat seal to polyethylene in a medical device.
SMST 2024
May 6-10, 2024
Eurofins EAG Laboratories will be presenting “Thermal Oxide Characterization – Heat Treat Modality vs. Composition“ on May 10th. We hope to see you there!
Stainless Steel Corrosion: Medical Device Applications with Auger
Auger Electron Spectroscopy (AES) is effective in determining the quality of passivation layers to prevent corrosion in medical devices.
Surface Characterization of Antibacterial Coated Sutures
Cold stage analysis has been shown to be effective for samples that are not solids at room temperature or that have components that are volatile in a vacuum system, such as the antibacterial coated sutures.
Testing Face Masks for Volatile Organic Compounds (VOCs)
Analytical methodology to evaluate a variety of different face masks for a class of chemicals known as volatile organic compounds
The Conspicuous Case of the Missing T0 in ISO 10993-5 Cytotoxicity Testing
In the world of medical device safety testing, ISO 10993-5 plays a crucial role. A key aspect of this, which is sometimes overlooked in certain studies, is the T0 time point, or time zero.
Understanding LA-ICP-MS for Microanalysis
LA-ICP-MS is a technique that uses direct micro-scale sampling to provide high precision elemental characterization of solid materials.
Weathering Polymeric Films
Polymeric films used in an outdoor application experienced reduced adhesion over time. The client suspected that UV degradation was occurring.
When Innovation Meets Failure Analysis
In our interconnected and changing world, it is important to know how to respond to potential electronic system failures.