Step 01
Sourcing
Direct partnerships with manufacturers in Turkey, Europe and Asia. Every candidate device is evaluated on clinical evidence, build quality and after-sales serviceability.
Import / Export
A regulated, transparent cross-border process.
From manufacturer selection to on-site installation, we manage every step of the import/export process between Iran, Switzerland and Turkey — with the documentation, certifications and technical support that clinics and distributors require.
Iran
Switzerland
Turkey
Six stages from origin to clinical use.
Step 02
Certification & compliance
CE marking review, technical file verification and alignment with medical device regulations for each destination market.
Step 03
Logistics & shipping
Multi-modal freight (air, sea, road) between our three operating countries with insured, temperature-safe transport when required.
Step 04
Customs assistance
Full customs clearance and administrative handling — HS classification, permits, import licenses and local registration.
Step 05
Delivery & installation
On-site delivery, installation by certified technicians, functional testing and operator training.
Step 06
Timelines
Standard lead times of 3–8 weeks from order confirmation, depending on manufacturer availability and destination market.
Regulatory
CE marking and medical device compliance.
Every device in our catalogue is CE-marked in accordance with the European Medical Device Regulation. We maintain a complete technical file for each platform and provide destination-specific documentation to support local registration and clinical use.
- CE marking under MDR (EU) 2017/745 where applicable
- Declaration of Conformity and technical documentation
- ISO 13485 quality management from source manufacturers
- Country-specific import permits and registrations
- Post-market surveillance and vigilance support