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Testing & compliance

Validation & safety testing for your equipment.

Autoclave and ultrasonic bath validation, pressure vessel inspection and medical electrical safety testing in Ireland and Northern Ireland.

Autoclave with a laptop and measurement device on top.

Autoclave validation

Validation of steam sterilisation equipment and processes, with the test programme based on the steriliser, intended loads and manufacturer requirements.

BioSonic ultrasonic cleaning bath on a worktop.

Ultrasonic bath validation

Validation testing for ultrasonic cleaning baths used in dental practices, with findings documented for the equipment tested.

Pressure vessel inspection

Examination and reporting for pressure equipment, based on the installation and applicable Irish in-service requirements.

Medical electrical safety

Recurrent safety testing and testing after repair of medical electrical equipment and systems, using methods appropriate to the device and manufacturer instructions.

Standards & regulatory references

Technical references
for equipment testing.

The standards and regulations relevant to the services above.

Medical electrical safety

IEC 62353

The reference for recurrent safety testing and testing after repair of medical electrical equipment and systems.

View IEC reference

Sterilisation validation

EN ISO 17665

Requirements for the development, validation and routine control of moist-heat sterilisation processes for medical devices.

View ISO reference

Steam steriliser performance

EN 13060 / EN 285

Performance and testing references for small steam sterilisers and large steam sterilisers respectively, according to equipment type.

Irish pressure systems

Part 10 & Schedule 12

Irish General Application Regulations governing pressure systems, including relevant examination and reporting requirements for pressure vessels.

View HSA guidance
How these references apply to your equipment

The applicable standard, edition, test method and reporting scope depend on the device, its intended use and the manufacturer’s instructions. Medical electrical testing requirements do not automatically apply to every beauty or salon device. Confirm the relevant scope when arranging a service.

The EU Pressure Equipment Directive 2014/68/EU concerns the design, manufacture and conformity assessment of pressure equipment within its scope. It is distinct from Ireland’s in-service pressure-system examination requirements.

These references describe the technical and regulatory context; they are not a claim of organisational accreditation or blanket certification.

Testing arrangements

Choose the testing service.

Use the contact form to request validation, pressure vessel inspection or electrical safety testing. Previous reports and manufacturer documentation help establish the appropriate testing programme.

The test methods and reporting requirements are confirmed for the equipment and site before the visit, including the applicable requirements in Ireland or Northern Ireland.

Arrange validation or safety testing.

Contact Adimevo to discuss the testing your equipment needs.

Request testing