PRATICIMA (PRATICIMA)
Praticima - Innovative solutions for medical equipment | 40 years of expertise
Discover Praticima, the leader in medical equipment solutions. For more than 40 years, we have designed and manufactured innovative equipment for hospitals, clinics, and healthcare establishments. Explore our full range of carts, cabinets, tables, and accessories to improve the quality of care and optimize your medical environment.
- Type
- Manufacturer
- Location
- Reyrieux, France
- Founded
- 1992
- Website
- praticima.fr
- Categories
- 医療およびヘルスケア用品
Listed in a source registry
France INSEE Sirene / INPI RNE state register (annuaire-entreprises.data.gouv.fr)
Verified facts
- lei-lapsed (amber), checked 2026-08-07 GLEIF global LEI register (golden copy)
- registry-active-global (green), checked 2026-08-07 France INSEE Sirene state register (data.gouv.fr bulk file)
- registered-manufacturer (green), checked 2026-08-07 France INSEE Sirene state register (data.gouv.fr bulk file)
- registry-id-verified (green), checked 2026-07-22 Annuaire des Entreprises (INSEE / INPI)
- places-goods-on-market (green), checked 2026-08-09 Registre national des producteurs (ADEME/SYDEREP), France
- sanctions-clear (green), checked 2026-07-26 OpenSanctions
- bodacc-accounts-filed (green), checked 2026-07-26 BODACC (annuaire-entreprises)
- directors-on-file (green), checked 2026-07-26 INSEE Sirene (annuaire-entreprises)
- export-registered (green), checked 2026-07-26 EU EORI validation (European Commission)
- debarment-clear (green), checked 2026-07-26 OpenSanctions
- vat-valid (green), checked 2026-07-31 VIES (European Commission)
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)