Europlaz Technologies


Europlaz is a UK-based leading medical device contract manufacturer with over 40 years of experience in design, engineering, and manufacturing for the medical device industry. They specialize in producing high-quality plastic injection moulding parts, sub-assemblies, and finished medical devices, supporting the entire product lifecycle from concept to market. Europlaz is ISO 13485 certified and FDA-compliant, offering flexible, resourceful, and comprehensive solutions to clients ranging from start-ups to international blue-chip companies. They focus on innovation, quality, regulatory compliance, sustainability, and agile manufacturing processes, ensuring rapid prototyping, scalable production, and full regulatory support.

Industries

health-care
manufacturing
medical-device

Nr. of Employees

medium (51-250)

Europlaz Technologies

Southminster, Essex, United Kingdom, Europe


Patents

Respiratory gas flow sensor with sampling port

US-9999741-B2

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Products

Actuators and inhaler components

Injection-moulded components and sub-assemblies used in actuators and inhaler systems (examples of contract manufacturing work).

Drug/device combination products

Multi-component devices combining drug delivery and device functionality, assembled and validated for clinical use.

Auto-injector kits and pre-filled component holders

Assembly and production of auto-injector kits and pre-filled component holders for self-administration or clinical use.

Non-invasive sensors and single-use disposables

Manufacture and assembly of disposable sensor components and single-use medical disposables for diagnostic and monitoring applications.

Operating-room kits and pouching

Complete kits for operating-room procedures including printed labels, pouching and finalised packaging for surgical consumables.


Services

Turnkey design, engineering, prototyping, tooling, validation and production services to take medical device concepts to market-ready products.

Tool design, commissioning, maintenance and injection moulding of medical-grade polymer components across a fleet of machines and a broad range of clamp forces, supporting precision and scalable volumes.

Assembly and sub-assembly of medical and diagnostic devices in ISO Class 7 cleanrooms with environmental monitoring, validated processes and traceability.

Validation testing, ISIR and capability reporting, FAI, Gage R&R and other verification services to support device release and regulatory submission.

Sterilisation services and coordination as part of the manufacturing and supply chain to ensure final products meet sterility requirements, working with specialist subcontractors.

Packaging design, labelling, pouching and final kitting services to prepare devices for distribution and clinical use with regulatory-compliant labeling and batch control.

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Expertise Areas

  • Medical device contract manufacturing
  • Cleanroom manufacturing and controlled-environment assembly
  • Injection moulding and tooling for medical polymers
  • Design for manufacturability (DFM) and project engineering
  • Show More (9)

Key Technologies

  • Injection moulding (medical-grade thermoplastics)
  • All‑electric injection moulding presses
  • Insert and over‑moulding
  • Two‑shot / multi‑shot moulding
  • Show More (7)

News & Updates

Europlaz has expanded its production facilities with a £200,000 investment, adding 200m² of ISO Class 7 cleanroom space.

Europlaz discusses the importance of single-use medical devices in healthcare for safety, cost, and sustainability.

Europlaz provides a comprehensive guide on regulatory compliance in medical device manufacturing.

Katy O’Keeffe, Strategy Director, recognized as an ‘Exemplar’ in the Top 100 UK Manufacturers 2025.

Guidance on CE marking for medical devices to ensure EU safety compliance.

Europlaz's partnership with Edinburgh Genetics to manufacture antibody test kits during the COVID-19 pandemic.

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