We protect medical device safety and integrity through advanced sterilization methods and ISO-certified cleanroom packaging processes.
A high-reliability sterilization process designed to eliminate microbial life and support patient safety.
Ideal for heat- and moisture-sensitive medical devices. Our gas diffusion process reaches complex geometries and integrated components without compromising material integrity.
With our ethylene oxide (EO) sterilization infrastructure, we provide reliable, validation-supported sterilization services for medical product manufacturers. Our processes are controlled in line with international standards, with product safety, biocompatibility, and repeatability at the core. We deliver integrated solutions that provide traceability and quality assurance throughout customers' sterilization workflows.
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Our controlled environments exceed industry expectations for particle count and pressure differential.
Continuous monitoring systems retain 99.99% of particles down to 0.3 microns.
Routine microbial sampling and environmental trend analysis help maintain sterility assurance.
The final barrier between your medical device and potential contamination. We design packaging that withstands demanding conditions.
Product Receipt and Preparation. Before packaging, products are checked for batch information, physical integrity, and process suitability.
Primary Packaging. Medical-grade barrier packaging is selected and applied according to product geometry and sterilization method.
Seal Control. Heat-sealing parameters are verified; seal integrity, peel strength, and visual quality checks are performed.
Labeling and Traceability. UDI, lot, and barcode information secure traceability after packaging.
Partner with DLR Medikal for custom sterilization and packaging solutions tailored to your product requirements.
