Pure medtech. Every stage. One partner.
Perdigó Medical works exclusively in medical devices, developing premium products for MedTech innovators worldwide
Developing the next generation of medical devices, which will change the paradigm in healthcare: focus real world health outcomes, usability engineering, and new technologies hold some of the keys to unlock this future.
Engineering new IVD devices and technologies that push the boundaries of and democratise access to diagnostics.
Improving health outcomes by empowering patients and healthcare professionals alike, we deliver solutions for remote patient monitoring, connected medical devices and digital health platforms.
New medical devices and technology platforms to optimise each step of the IVF process in terms of both success rate and cost efficiency.
Understanding surgeons’ needs and wishes, we deliver innovative and reliable surgical instruments that minimise patient risk and facilitate a speedy recovery.
World-class experts in drug delivery medical devices: inhalation (soft mist and dry powder), parenteral, and ophthalmic delivery routes.
Engineering new biotechnology platforms for gene editing, cell therapy and synthetic biology to enable groundbreaking treatments.
When standard solutions are not available to perform a process, whether in research, production, quality control or other applications, Perdigó develops custom fixtures, instruments and machines.
End-to-end medical device engineering, from concept to market. Plug in at any stage.
Definition of the product concept, intended purpose, user profile, and regulatory context.
Translating user needs into technical requirements and develop proof of concept prototypes.
Integration and refinement of design solutions across mechanics, electronics, firmware, and more.
Production of initial device units for validation and usability testing.
Verifying that the design meets all specified requirements through software testing, usability evaluations, and risk control checks.
Conducting usability validation, clinical evaluations, and risk file review to ensure we have built the right device.
Thorough, MDR-compliant technical documentation to support your CE marking submission.
Smooth transition into manufacturing with our network of vetted partners.
Continued compliance and IP support as the product moves toward commercialisation and beyond.
Perdigó Medical covers the full range of work a medical device demands, from the several engineering disicplines to IP and regulatory strategy. Explore them all below:
Structural design, component tolerancing, and assembly development for reliable device performance.
Learn moreCircuit design, PCB layout, and hardware integration for active medical devices.
Learn moreUser-centred design for safe and effective devices. Formative and summative evaluations structured to IEC 62366-1, planned from day one.
Learn moreUser-centred form development balancing ergonomics, brand, and manufacturability.
Learn moreFunctional prototypes from proof-of-concept through design verification at each development stage.
Learn moreISO 14971-compliant hazard identification, risk estimation, and risk-benefit analysis across the device lifecycle.
Freedom-to-operate analysis, patentability assessments, and filing strategy during development.
Pathway selection and submission planning for the EU and US markets, from early design through filing.
Perdigó Medical offers end-to-end medical device development for innovators who want real outcomes with the least friction and risk. From conception and design to regulatory compliance and market launch, our experts accompany you every step of the way.
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medtech sectors
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engineering disciplines
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team