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Customer success: Validated excellence in global plastic injection moulding for MedTech

Explore how MouldFlo partners with leading machine makers, medical device manufacturers, and contract manufacturing organizations to solve the complex technical challenges of modern injection moulding.

// How MouldFlo improves production

Stories from real production lines

Co-innovation with global industry leaders

MouldFlo’s position as a first-mover in digital flow monitoring since 2014 is the result of deep technical co-production. We don’t just supply hardware; we innovate alongside the best in the industry.

  • MedTech & pharma: We have co-developed validation standards with world-leading pharmaceutical company to support their production meets the most stringent MDR and FDA requirements.

  • High-precision consumer goods: Our partnership with world-renowned toy manufacturer has pushed the boundaries of high-volume efficiency and sustainable, cost-controlled production.


The Result?
A transparent production environment where “the cooling circuit” is no longer a hidden variable, but a validated data stream.

// Frequently asked questions

Technical Q&A

If you do not find the answer to your question, please reach out to our team

MouldFlo allows CMOs to offer their customers higher levels of process capability and automated validation reports. By using OPC UA and Euromap 82.1, CMOs can prove to their customers that every part was produced within the validated thermal window, providing a significant competitive advantage in the MedTech sector.

A machine-agnostic approach allows for standardization of monitoring and validation procedures across a diverse fleet of IMM brands (Arburg, Engel, Netstal, etc.). This ensures that a “Digital Fingerprint” established in one country can be perfectly replicated at another production site, regardless of the local machine brand.

Automated documentation removes human error from the reporting process. For MDMs, this means that every production run is backed by a continuous, digital audit trail of flow, temperature, and pressure, which is instantly accessible during ISO 13485, MDR or FDA inspections.

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// Get a quote

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Reply within 2 business days · Used in 30+ countries · No commitment

// Get a quote

Contact MouldFlo

Fill in the form below and we will get back to you shortly.

Reply within 2 business days · Used in 30+ countries · No commitment