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Standards & Approvals

It is our policy to design and manufacture equipment of the highest quality and reliability to meet the requirements of our customers. Moor Instruments has been assessed and certified as meeting the requirements of ISO13485:2003 by the Standards Council of Canada Accredited Registrar, ISO13485:2003 by UKAS Quality Management and Directive 93/42/EEC CE 0120. By working to strict quality control procedures, we ensure product safety and reliability.

Moor Instruments FDA 510(k) registered products

The following Moor Instruments products are registered with the FDA (Federal Device Agency) :-

DRT4™ - 510(K) Number K011070
moorLDI™ - 510(K) Number K980383
moorLDI-IR™ - 510(K) Number K032841
moorLDI2-BI™ - 510(K) Number K060976
moorLDLS™ - 510(K) Number K063561
moorFLPI™ - 510(K) Number K063586
moorVMS-LDF1™ & moorVMS-LDF2™ - 510(K) Number K083082
moorVMS-PRES™ - 510(K) Number K102433

Moor Instruments CE marked products

The following Moor Instruments products are CE (European Conformity) marked :-

DRT4™
IRLD20™
MIC2™
moorFLPI™
moorLAB™
moorLDI™
moorLDI2-2λ™
moorLDI2-BI™
moorLDI2-IR™
moorLDI2-VR™
moorVMS-LDF™
moorVMS-PRES™
moorVMS-DAQ™
moorLDLS™
moorLDLS2™
PRM2™
SH02™

Moor Instruments licensed Health Canada products

The following Moor Instruments products are licensed by Health Canada :-

moorLDI2-BI™ Licence No. 75477
DRT4™ Licence No. 34936
moorFLPI™ Licence No. 80750
moorLDI2™ Family Licence No. 79095

The moorLDI2™ family consists of the following:

• moorLDI2-IR™
• moorLDI2-VR™
• moorLDI2-2λ™
• moorLDI2-HIR™
• moorLDI2-HR™
• moorLDI2-II™

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