Independent certification in accordance with the Marine Equipment Directive (2014/90/EU)

DCI Group conducts independent conformity assessments for maritime equipment on board seagoing vessels under the Marine Equipment Directive (MED). We assess products for conformity with Directive 2014/90/EU and the associated international standards and IMO requirements.

With a structured and transparent working method, we ensure reliable and consistent certification of your products.

Certification of maritime equipment under the Marine Equipment Directive (MED)

DCI Group supports manufacturers and suppliers in demonstrating conformity with the Marine Equipment Directive (MED – 2014/90/EU) .

The MED sets requirements for maritime equipment installed on board ships sailing under the EU flag. Certification is required to demonstrate that products comply with applicable international standards and safety requirements.

What is the MED?
The Marine Equipment Directive (MED) is European legislation that sets requirements for equipment used on board seagoing vessels.

The MED sets requirements for maritime equipment installed on board ships sailing under the EU flag. Certification is required to demonstrate that products comply with applicable international standards and safety requirements.

The guideline aims to:

  • ensuring safety at sea
  • harmonizing requirements within the EU
  • ensuring compliance with international IMO standards

Products covered by the MED must be assessed by an independent certification body.

For which products?

DCI Group focuses on the certification of, among others:

  • Rescue equipment (select categories)
  • Lifeboat equipment
  • Propulsion systems for auxiliary and rescue vessels

Certification modules

Certification under the MED is carried out according to standardized modules.

DCI Group performs certification activities for:

Module B – EU type examination

Review and approval of the product design.

Module F – Conformity with type

Verification that produced products correspond to the approved type.

Together, these modules form the basis for demonstrating conformity.

Certification process

The certification process consists of:

  1. Application and intake
  2. Assessment of technical documentation
  3. Evaluation and testing (if applicable)
  4. Independent review
  5. Certification Decree
  6. Issuance of certificate

The process is structured in accordance with ISO/IEC 17065 and ensures objective and consistent decision-making.

Independence and reliability

DCI Group operates as an independent third party and guarantees that:

  • certification decisions are based on objective evidence
  • Conflicts of interest are prevented
  • evaluation and decision-making are strictly separated

Accreditation status

DCI Group is currently undergoing the accreditation process with the Dutch Accreditation Council (RvA) and is not currently accredited.

Interested?

Would you like to know if your product falls under the MED, or would you like to start a certification application? Contact us!

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Request a quote for MED certification?

MED Module B

EU type examination, type approval (Wheelmark)

MED Module B

MED Module F

Product verification, batch/product inspection (Wheelmark)

MED Module F

MED Combination Modules B+F

Type testing + product verification, full Wheelmark certification

MED Combination Modules B+F

Independent and expert

We assess objectively in accordance with recognized standards and oversight frameworks. DCI Group is currently undergoing the accreditation process and operates according to the requirements of ISO 17065, so you can trust the outcome.

Clear process and fixed steps

You know exactly what information needs to be provided, which steps are involved during the assessment, and what you will receive upon completion.

Specialist in RCD-CE and MED certification

Independent certification and inspection in accordance with European guidelines for the maritime sector.

Ready for certification? We will help you.

Apply for your certification immediately
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