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Certifications

Providing safety and security with every medical device we produce

ISO 13485:2016

At Lucas Lifecare, we are proud to announce that our manufacturing facility has obtained ISO 13485 certification, the globally recognized standard for medical device quality management systems.

This achievement reflects our commitment to:

  • Excellence in Manufacturing – Consistent processes built on precision and safety.

  • Global Compliance – Alignment with international regulatory requirements.

  • Trust & Reliability – Delivering products that healthcare professionals can depend on.

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Standards, Tests & Certifcations for LifeUltra:

  • EN 61010-1: 2010 / AM1:2016 / COR1:2019"

  • 61010-1 Edition 3.1 2017-01 CONSOLIDATED VERSION

  • IEC 61010-2-040:2021EN

  • IEC 61326-1: 2021

  • IEC 61326-1 Edition 3.0 2020-10

  • EN 13060:2014+A1:2018

  • AAMI ANSI ST 55 : 2016

  • AAMI ANSI ST55:2016/(R)2023

  • IEC 62304:2006

  • ASME BPVC Sec VIII, Div I: 2019

  • CFR 47, FCC Part 15B (using ANSI C63.4: 2014)

  • ISO 62366-1

  • IEC 62366-1 Edition 1.1 2020-06 CONSOLIDATED VERSION

  • ISO 17665:2024

  • ISO 17665 First edition 2024-03

  • IEC 60601-4-2

  • IEC 60601-1-2 ed 4.1

  • IEC TR 60601-4-2 Edition 1.0 2016-05

  • IEC 60601-1-2:2014+AMD1:2020 CONSOLIDATED VERSION edition 4.1

Image by Markus Gjengaar

Standards, Tests & Certifcations for LifeRay:

FDA Cleared for LifeRay

  • IEC 60601-1 Safety requirements for Medical Electrical Systems

  • IEC 60601-1-2 Electromagnetic disturbances  for Medical Electrical Systems

  • IEC 60601-1-3 Radiation protection in Diagnostic X -ray Equipment

  • IEC 60601-2-28 X-ray tube assemblies for medical diagnosis

  • IEC 60601-2-65 Dental intra-oral X -ray Equipment

  • IEC 62304 ed 1.1 Software life cycle  processes  for Medical Devices

  • IEC 62366-1 ed 1.0 Usability Engineering Application Medical Devices

  • 21CFR sub chapter-J FDA Radiological Health Regulation

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