PLASTIC BILLAT
Billat nhựa - Chuyên gia về ép nhựa cho nguyên mẫu và dòng công nghiệp nhỏ
Plastic Billat, chuyên gia về ép nhựa và gia công nhựa tại Pháp từ năm 1973. Pháp sản xuất các bộ phận kỹ thuật cho công nghiệp. Yêu cầu báo giá miễn phí của bạn!
- Type
- brand seeking distribution
- Location
- GAMACHES Somme, France
- Founded
- 2012
- Website
- https://plasticbillat.fr
- Categories
- Vật tư và thiết bị nha khoa
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)