PLASTIC BILLAT
Plastic Billat - Experten für Kunststoffspritzguss für Prototypen und kleine Industrieserien
Plastic Billat, Spezialist für Kunststoffspritzguss und Kunststoffverarbeitung in Frankreich seit 1973. Französische Herstellung technischer Teile für die Industrie. Fordern Sie Ihr kostenloses Angebot an!
- Type
- brand seeking distribution
- Location
- GAMACHES Somme, France
- Founded
- 2012
- Website
- https://plasticbillat.fr
- Categories
- Dentalbedarf & -geräte
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)