Certified. Documented. Verifiable.
Aprikos Medical is a Norwegian manufacturer of surgical instruments and medical furniture. Every product is designed, manufactured and released under a certified quality management system.
Quality is the product
For a surgical instrument there is no such thing as “good enough”. Our quality focus runs from design and manufacturing to post-market follow-up of every batch we release — and our Code of Conduct sets the same standard for how we do business as for what we make.
Patient safety first
Every decision is measured against one standard: safe use in the operating theatre. Vigilance, complaint handling and post-market surveillance under MDR 2017/745.
Code of Conduct
Anti-corruption, fair competition, labour and human rights. Signed by every employee — and required of every manufacturing partner and supplier we work with.
Full traceability
Every product is traceable by article and batch, from raw material to delivered order — UDI-labelled in line with MDR requirements.
Environmental responsibility
ISO 14001-certified environmental management — responsible material choices, reduced packaging and lower-impact logistics across the supply chain.
Continuous improvement
Internal audits, CAPA and management review keep the quality system alive — a working tool in daily operations, not a binder on a shelf.
Certificates & documentation
MDR 2017/745
8,000+ codes certified. Notified body NB XXXX.
ISO 13485:2016
Quality management for medical devices.
ISO 14001
Environmental management system.
CE marking
EU health, safety and performance conformity.
Multi-source manufacturing, one quality system
Manufacturing partners in Germany, Türkiye and Pakistan — every product qualified, quality-assured and released under our Norwegian ISO 13485 quality system.
Document vault — restricted access
Certificates, Declarations of Conformity, IFU and technical files are available to registered distributors, hospitals and tender officers.
| Document | Type | Scope | Valid to | Access |
|---|---|---|---|---|
| EC Certificate — MDR 2017/745 | Full portfolio | 2030 | ||
| ISO 13485:2016 certificate | Design & manufacture | 2029 | ||
| Declaration of Conformity — General Surgery | Class I / Is | — | ||
| IFU & reprocessing instructions | All instruments | — | ||
| Tender documentation pack | ZIP | Procurement | — | |
| Code of Conduct | Public | — | Open ↓ | |
| Certification summary (1 page) | Public | — | Open ↓ |
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