Oertli Instrumente AG
- Type
- brand seeking distribution
- Location
- Berneck, Switzerland
- Website
- https://oertli-instruments.com
- Categories
- Medische en gezondheidszorgbenodigdheden
- Markets
- Zwitserland
Listed in a source registry
Verified facts
- domain-registered (green), checked 2026-08-23 Domain registry record
- operating-permit (green), checked 2024-06-17 SHAB, Swiss Official Gazette of Commerce
- registered-manufacturer (green), checked 2026-08-22 Agencia Estatal de Medicamentos y Tecnologias en Salud (AGEMED, Bolivia), listado oficial de registros sanitarios aprobados
- registry-active-global (green), checked 2026-08-31 SHAB, Swiss Official Gazette of Commerce
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)