ECAS / MOIAT Conformity Assessment (Where Separately Applicable)

ECAS is the Emirates Conformity Assessment Scheme administered through the UAE Ministry of Industry and Advanced Technology (MOIAT). It is a separate conformity-certification route for products subject to MOIAT technical regulations; it is not the MOHAP medical-device registration portal. For a medical-device project, NKB Regovanta screens whether ECAS is separately relevant and aligns documentation so MOIAT and MOHAP pathways never contradict.

Assess ECAS / MOIAT Applicability

When This Support Is Needed

A medical device or accessory includes electrical, low-voltage (LVD), or wireless radio components regulated by MOIAT

Screening whether finished equipment or accessories require separate ECAS Certificate of Conformity (CoC)

Addressing UAE customs inquiries regarding MOIAT / ECAS compliance for imported medical electronics

Harmonizing accredited laboratory test reports between MOHAP registration files and MOIAT requirements

What We Challenge Before Submission

Is ECAS applicable to the finished medical device or only to specific power adapters and electrical sub-components?

Do test reports originate from ILAC-accredited or IECEE CB Scheme laboratories recognized by MOIAT?

Is there total consistency between product ratings on the ECAS application, MOHAP file, and device labels?

Does the local UAE trade entity have the appropriate commercial license activities for ECAS issuance?

Is the ECAS Certificate of Conformity kept active to prevent shipment holds at UAE customs ports?

Our MOIAT / ECAS Advisory Scope

ECAS / MOIAT technical regulation applicability screening for medical products and electrical modules

Product-scope and mandatory standard review (Low Voltage, RoHS, Energy Efficiency, Wireless / TDRA)

Accredited ISO/IEC 17025 laboratory test-report readiness and CB Scheme certificate review

UAE commercial trade license and local applicant interface coordination

Certificate of Conformity (CoC) electronic application preparation and documentation filing

Alignment of MOIAT conformity evidence with MOHAP medical equipment technical files

ECAS annual renewal planning and regulatory lifecycle maintenance

Resolution of UAE customs and border inspection queries regarding ECAS certification

Distinction Clarification:

MOHAP medical equipment registration and MOIAT/ECAS are separate regulatory systems. We ensure that electrical safety, EMC, and wireless evidence submitted to MOIAT are completely aligned with the medical device technical file submitted to MOHAP.

Screen and Secure MOIAT / ECAS Conformity for Regulated Components

Our UAE conformity engineers assess ECAS applicability, review CB Scheme reports, and obtain Certificates of Conformity.

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