Orthotechniq
Ivorian producer of medical supplies, on the national commercial register.
Orthotechniq is registered in Cote d'Ivoire under RCCM number CI-ABJ-03-2021-B12-04092. The registration document filed with the commercial court of Abidjan records the activity as: La conception et la fabrication d'orthèses médicales et plus précisément tout appareil orthopédique destinés à. Place of business on the filing: BIETRY EN FACE DU COLLEGE NOTRE DAME D'AFRIQUE ; 01BP1330ABIDJAN01. Every fact on this card comes from that filing, which is linked as the source.
- Type
- brand seeking distribution
- Location
- Abidjan, Côte d'Ivoire
- Categories
- 医療およびヘルスケア用品
- Markets
- コートジボワール
Listed in a source registry
Registre du commerce et du credit mobilier (RCCM), Tribunal de commerce d'Abidjan
Verified facts
- registry-id-verified (green), checked 2026-08-20 Registration filing, Tribunal de commerce d'Abidjan (RCCM)
- registry-activity (green), checked 2026-08-20 Registration filing, Tribunal de commerce d'Abidjan (RCCM)
- registered-address (green), checked 2026-08-20 Registration filing, Tribunal de commerce d'Abidjan (RCCM)
- facility-registered (green), checked 2026-08-20 Registration filing, Tribunal de commerce d'Abidjan (RCCM)
- debarment-clear (green), checked 2026-09-01 OpenSanctions
- sanctions-clear (green), checked 2026-09-01 OpenSanctions
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)