Certified to ISO 13485. Developed and manufactured in Germany
At Medintim, quality isn’t optional—it’s built in. Our ISO-certified quality management system (ISO 13485) governs how we design, manufacture, and support every product. Independent audits, risk management, and supplier controls turn promises into measurable, repeatable results.
Manufacturing in Germany gives us tight end-to-end control: engineering sits next to production for faster improvements, inputs come from vetted European suppliers, and full batch traceability ensures the product you buy today performs like the one you buy next year.
For clinicians and pharmacies, that means predictable performance, clear instructions, audit-ready documentation, and reliable supply. For consumers, it means safe, skin-friendly materials, consistent quality, and straightforward guidance.
Our continuous quality loop—design and risk assessment through supplier qualification, in-process checks, final release, and post-market surveillance—feeds real-world insights back into better products. We also prioritize durability, responsible sourcing, and efficient production to reduce waste. In short: ISO keeps our quality auditable; Made in Germany keeps it repeatable.
Frequently Asked Questions
What does ISO 13485 mean for healthcare professionals?
ISO 13485 is the medical-device standard for quality management. It ensures design controls, risk management, traceability, and post-market surveillance so performance is consistent in real-word use.
How does "Made in Germany" improve reliability?
Co-located engineering and production shorten feedback loops, vetted suppliers ensure material integrity, and batch-level documentation enables fast investigations and continuous improvement.
Are Medintim products the same across batches?
Yes—specification checks at incoming, in-process, and final release keep batches consistent. Traceability links every finished product to its materials and tests.
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