Products
Back
Products
Core Disciplines
Chemistry Immunoassay Hematology Urinalysis Microbiology Blood Banking Protein Chemistry Service
Workflow & Informatics
Automation Systems Clinical Information Management Tools PROService Remote Service Tool DxONE Inventory Manager Instrument Aggregator Middleware Data Analytics
Solutions For
Pioneering Digital Hematology Clinical Decision Support - TriageGO SARS-CoV-2 Antibody Testing Anemia Cardiovascular Disease Diabetes Diagnostics Drug Monitoring & Detection Prostate Cancer Detection Reproductive Health Sepsis Life Sciences ›
Support
Back
Support
Account Support
Create Account Manage Account Settings View All Account Support
Product Support
DxS Service In Vitro Diagnostic Regulation (IVDR) Manage My Technical Documents Search for Technical Documents Safety Data Sheets (SDS/MSDS) Search for Software Downloads Technical Documents Overview Manage My Regulatory Notifications Manage My Warranties & Agreements Request Instrument Support View Services Information View All Product Support Access Quality Assurance Programs
Ordering Support
Order Status & Tracking Track My Invoices View Return/RMA Policy Get Help with Orders View All Ordering Support
Resources
Back
Resources
Product Training
Training Courses › Register for Training ›
Education & Research
Webinars Posters 3D Virtual Laboratory Showcase
Insights
Clinical Studies & Trends Case Studies Publications
Company
Back
Company
People & Culture
Overview Meet Our Teams Diversity + Inclusion How We Work Innovation
Careers
Job Search › Career Stories Programs & Grants Office Locations
News & Events
Awards & Recognition Newsroom Blog Events Calendar
Home / Support / In Vitro Diagnostic Regulation (IVDR)

In Vitro Diagnostic Regulation (IVDR)

What is In Vitro Diagnostic Regulation (IVDR)?

In Vitro Diagnostic Regulation (IVDR – 2017/746) replaces the existing In Vitro Diagnostic Directive (IVDD – 98/79/EC). The E.U. legislation was updated to keep up with technical advances and changes in medical practice to create a more robust, transparent, and sustainable regulatory framework. Beckman Coulter is working to ensure all relevant products are covered under the new ordinance.

What is covered under IVDR?

Any in vitro diagnostic medical device that is a reagent, reagent product, calibrator, control material, kit, instrument, apparatus, piece of equipment, software or accessory, whether used alone or in combination, intended by the manufacturer to be used in vitro for the examination of specimens, including blood and tissue donations, derived from the human body, solely or principally to provide information on one or more of the following:

  • Concerning a physiological or pathological process or state
  • Concerning congenital physical or mental impairments
  • Concerning the predisposition to a medical condition or a disease
  • To determine the safety and compatibility with potential recipients
  • To predict treatment response or reactions
  • To define or monitoring therapeutic measures

Specimen receptacles shall also be deemed to be in vitro diagnostic medical devices.

What is the difference between IVDR and IVDD?

Some of the main differences between the new In Vitro Diagnostic Regulation and the previous In Vitro Diagnostics Directive are: 1,2

  • Scope and classification of products
  • Improved transparency and data for the European Database for Medical Devices (EUDAMED), the European Union’s database for medical devices
  • Role of Economic Operators (clarification of obligations of manufacturers, authorized representatives, importers and distributors)
  • Changes to notified bodies
  • Addition of Unique Device Identification (UDI) System for every IVD device
  • Changes to clinical evaluation processes with an increase in clinical evidence and conformity assessment

Device risk-classification categories

In the new IVDR classification system, devices will be divided into four categories based on the intended purpose of a device and its inherent risk level, with class A posing the lowest risk to the patient and class D being the highest risk to the patient and the public:

  • Class A
    Risk level: Low

    Review process:
    Manufacturer self-declaration

    Examples:
    General lab instruments, specimen receptacles

  • Class B
    Risk level: Low-Moderate

    Review process:
    Notified body review required

    Examples:
    Some self-test products such as pregnancy, fertility, cholesterol and devices that detect glucose

     

  • Class C
    Risk level: Moderate-High

    Review process:
    Notified body review required

    Examples:
    Cancer tests, genetic tests, congenital screening of embryos, fetuses or new-born babies

     

  • Class D
    Risk Level: High

    Review process:
    Notified body review required

    Examples:
    High risk diseases, blood screening of blood components, determining the infectious load of a life-threatening disease

     

What is the IVDR implementation timeline?

The IVDR implementation timeline varies based on product class.3

IVDR General Playbook

How does this impact me as a customer?

Beckman Coulter is working to ensure all relevant products are IVDR-compliant and have processes in place for recertification to ensure product continuity for all our customers.4

IFU Changes
IFUs will be updated to include the CE Notified Body Number alongside the CE mark.

Other changes to IFUs may include:

  • Intended purpose statements
  • Warnings or contraindications
  • Additions or alterations to sample types, stability, interfering substances, linearity, reference ranges, specificity and sensitivity
  • Manufacturer’s telephone number
  • Updates to supporting references 

Labeling changes
You can expect to see changes to our product labeling. 

For vials, tubes and cartridges, you may see:

  • Addition of IFU symbol and web address for IFUs
  • Addition of phone number under BEC address
  • Addition of target fill volume
  • Removal of approximate concentration from vial labels
  • Removal of hazard codes

For product boxes, you will see the addition of the IVDR-required notified body number next to the CE mark.

 

Beckman Coulter Diagnostics products that will be covered under IVDR


  • Clinical Chemistry Systems
    Clinical Chemistry Systems

    Reducing Total Cost of Ownership

    In today's changing healthcare climate, laboratories around the world are challenged to elevate patient care and reduce operating costs at the same time. The low cost of ownership of our clinical chemistry analyzers help laboratories achieve their goals and manage resources effectively without compromising quality.

    Learn how
    your laboratory can:

    • Discover scalable solutions for laboratories of all sizes

    • Standardize processes

  • Immunoassay Systems
    Immunoassay Systems

    Scalability, Reliability and Simplicity

    Extend the services of your core laboratory with our range of immunoassay analyzers and comprehensive portfolio of assays. Whether you run dozens or thousands of tests per day, you can rely on the same innovation and quality in our immunoassay instruments and systems that you know and trust from the rest of our total laboratory solution portfolio.

    Learn how your laboratory can:

    • Scale with consistency

    • Count on high levels of reliability

    • Simplify the complex maintenance

    • Support improved patient care

  • Protein Chemistry Systems
    Protein Chemistry Systems

    Supporting Disease Diagnosis and Monitoring

    Are you seeking solutions that optimize and increase efficiency to advance patient care? Our protein chemistry analyzers combine the high performance needed to deliver fast, accurate results with the flexibility to accommodate a broad spectrum of laboratory preferences.

    Learn how your laboratory can:

    • Test with confidence

    • Choose the right option

    • Manage a range of diseases

    • Evolve with innovation

  • Hematology
    Hematology

    Comprehensive, High-quality Hematology Solutions

    Deliver precise, accurate results faster. Use our hematology analyzers to enhance your medical laboratory operations and improve patient care.

    Learn how
    your laboratory can:

    • Achieve accurate results quickly with automated repeat and reflex testing to reduce TAT

    • Reduce manual work, automate processes and use data management tools for auto-validation

    • Free up workspace

    • Make analytical testing more economical


  • Urinalysis
    Urinalysis

    Take the Subjectivity Out of Urinalysis

    Our selection of urine chemistry and urine microscopy analyzers help you significantly reduce your urinalysis laboratory's need for manual microscopic review and sample handling, thereby diminishing subjectivity and increasing test efficiency. 

  • Microbiology
    Microbiology

    Guide Critical Patient Decisions Using Proven Accuracy

    Impact treatment decisions with accurate detection of emerging antimicrobial resistance, improved workflow efficiency, expert consultation and top-ranked support.* Our selection of microbiology panels, systems and analyzers can enhance your laboratory’s productivity today and into the future.

  • Blood Banking
    Blood Banking

    Industry-leading throughput, high efficiency and reliable performance

    Our immunohematology and blood group testing analyzers and reagents deliver accurate results, while streamlining workflow and easing maintenance. Learn how your lab can experience industry-leading throughput, high efficiency and reliable performance.

  • Clinical Laboratory Automation Systems
    Clinical Laboratory Automation Systems

    Delivering Solutions Designed to Relieve Health System Pressure

    Expedite patient care and enhance laboratory efficiency with our automated clinical laboratory systems. Experience automated lab solutions that deliver excellence for today and expandability for tomorrow. 

References:

*MD Buyline. User Satisfaction Trending for Beckman Coulter Microbiology Systems. October 1, 2016.

1. 6 Major Differences Between EU’s MDR/IVDR and MDD/IVDD. (2019, March 14). RegDesk. https://www.regdesk.co/major-differences-eu-mdr-mdd/ 
2. FAQS: IN VITRO DIAGNOSTIC MEDICAL DEVICE REGULATION (IVDR). (2021). TUV. https://www.tuvsud.com/en-us/industries/healthcare-and-medical-devices/medical-devices-and-ivd/medical-device-market-approval-and-certification/eu-in-vitro-diagnostic-medical-device-regulation/faqs-in-vitro-diagnostic-medical-device-regulation-ivdr
3. https://www.medtecheurope.org/new-medical-technology-regulations/transition-periods/ accessed May 10, 2022
4. https://www.medtecheurope.org/wp-content/uploads/2020/05/20200526_Impact_Changes_Int_Reg_invitrodiagnostics_IVDR.pdf

 
Products
Support
Company Newsletter
Beckman Coulter Life Sciences
Stay Connected
Products
Support
Company
Newsletter
Beckman Coulter Life Sciences
Stay Connected

Information addressed to health professionals. The products presented on this site are for professional use only, and, where applicable, comply with the requirements of the IVD Directive 98/79 / EC. Instructions for use must be consulted before using these products.

 

© 2024 Beckman Coulter, Inc. All rights reserved. Beckman Coulter, the stylized logo, and the Beckman Coulter product and service marks mentioned herein are trademarks or registered trademarks of Beckman Coulter, Inc. in the United States and other countries.

U.S. Government Users Restricted Rights - As per GSA ADP Schedule Contract with Beckman Coulter, Inc., the use, duplication or disclosure is restricted as follows: Beckman Coulter hereby authorizes user to copy those documents published on the World Wide Web by Beckman Coulter, for noncommercial use, and only within the user's organization. Except as expressly provided above, nothing contained herein shall be construed as granting any license or right under any Beckman Coulter copyright. Nothing contained herein shall be construed as granting by implication, estoppel or otherwise any license or right under any patent or trademark of Beckman Coulter or any third party.