PLASTIC BILLAT
Plastic Billat - Expertos en Inyección de Plástico para Prototipos y Pequeñas Series Industriales
Plastic Billat, especialista en inyección y transformación de plásticos en Francia desde 1973. Fabricación francesa de piezas técnicas para la industria. ¡Solicita tu cotización gratuita!
- Type
- brand seeking distribution
- Location
- GAMACHES Somme, France
- Founded
- 2012
- Website
- https://plasticbillat.fr
- Categories
- Suministros y equipos dentales
Listed in a source registry
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-03 Mail server of the company domain
- domain-registered (green), checked 2026-08-03 Domain registry record
- fda-registered (green), checked 2026-08-03 FDA
- fda-contract-manufacturer (green), checked 2026-08-03 FDA
- debarment-clear (green), checked 2026-08-03 OpenSanctions
- sanctions-clear (green), checked 2026-08-03 OpenSanctions
- registry-active-global (green), checked 2026-08-03 INSEE Sirene (annuaire-entreprises)
- registered-since (green), checked 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- lei-lapsed (amber), checked 2026-08-23 GLEIF global LEI register (golden copy)
- financials-published (green), checked 2016-12-31 INPI/BCE published accounts (data.economie.gouv.fr)
- facility-registered (green), checked 2026-08-07 US FDA device establishment registration (openFDA)
- places-goods-on-market (green), checked 2026-08-30 Registre national des producteurs (ADEME/SYDEREP), France
- registry-activity (green), checked 2026-08-03 INSEE Sirene (annuaire-entreprises)
- directors-on-file (green), checked 2026-08-03 INSEE Sirene (annuaire-entreprises)
- registry-id-verified (green), checked 2026-07-15 Annuaire des Entreprises (INSEE / INPI)
- workforce-on-record (green), checked 2026-07-01 INSEE SIRENE (Registre national des entreprises)
Claimed certifications
- FDA Registered FDA Establishment Registration
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)