FCI SUD
Export Device to the United States But Perform No Other Operation on Device; Foreign Private Label Distributor; Manufact | Mapou Leclezio Goodlands Riviere Du Rempart | Mauritius
Verification
- Yes: Official registry Listed in openFDA device registration and listing (active manufacturers, sterilizers).
- Yes: Registration or licence number Record no. 3004467263 (issued by the source registry).
- No: Cross-source match Not found in another source.
- No: Website verified Website not checked.
Reputability score 60 of 100. A data-completeness and verification score, not a rating or endorsement. How it works
Details
- IndustryHub facility ID
- openfda:3004467263
- Category
- Medical equipment
- Sector
- Export Device to the United States But Perform No Other Operation on Device; Foreign Private Label Distributor; Manufact
- Activity
- Cannula, Ophthalmic; Cannula, Trocar, Ophthalmic; Conformer, Ophthalmic; Crutch, Ptosis; Dilator, Lachrymal; Forceps, Ophthalmic; Gauge, Measuring; Hook, Ophthalmic; Implant, Eye Sphere; Implant, Orbital, Extra-Ocular; Introducer, Sphere; K
- Location
- Mapou Leclezio Goodlands Riviere Du Rempart, Mauritius
- Country
- Mauritius
Data source
openFDA device registration and listing (active manufacturers, sterilizers). Licence: US government work, public domain (CC0).
Listings are not endorsements. IndustryHub does not verify, vet or vouch for any business. Buyers must do their own due diligence, confirm licences and certifications, and follow all export, import and sanctions laws.
