INFIPLAST
Accueil Industrie - Infiplast
Matériel médical et sous-ensembles thermoplastiques
- Type
- Manufacturer
- Location
- OYONNAX Ain, France
- Founded
- 1988
- Website
- https://infiplast.fr
- Categories
- Medische en gezondheidszorgbenodigdheden
Listed in a source registry
Verified facts
- fda-registered (green), checked 2026-08-03 FDA
- fda-contract-manufacturer (green), checked 2026-08-03 FDA
- sanctions-clear (green), checked 2026-08-03 OpenSanctions
- registry-active-global (green), checked 2026-08-03 INSEE Sirene (annuaire-entreprises)
- registry-id-verified (green), checked 2026-08-03 INSEE Sirene (annuaire-entreprises)
- registered-artisan (green), checked 2026-08-03 INSEE Sirene (annuaire-entreprises)
- registered-manufacturer (green), checked 2026-08-03 INSEE Sirene (annuaire-entreprises)
- directors-on-file (green), checked 2026-08-03 INSEE Sirene (annuaire-entreprises)
- debarment-clear (green), checked 2026-08-03 OpenSanctions
- facility-registered (green), checked 2026-08-03 US FDA device establishment registration (openFDA)
- domain-registered (green), checked 2026-08-03 Domain registry record
- corporate-mail-on-domain (green), checked 2026-08-03 Mail server of the company domain
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)