CREADENT MONTAUBAN (EMAIA)
의료 및 건강 관리 용품, 프랑스
CREADENT MONTAUBAN(EMAIA)은 프랑스 Montauban에 본사를 둔 의료 및 건강 관리 용품 회사입니다. 공공 사업 등록부에 등재되어 있습니다.
- Type
- brand seeking distribution
- Location
- Montauban, France
- Founded
- 2001
- Website
- https://emaia.fr
- Categories
- 의료 및 건강 관리 용품
Listed in a source registry
France INSEE Sirene / INPI RNE state register (annuaire-entreprises.data.gouv.fr)
Verified facts
- registered-since (green), checked 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- workforce-on-record (green), checked 2026-07-01 INSEE SIRENE (Registre national des entreprises)
- facility-registered (green), checked 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- web-presence-since (green), checked 2026-08-21 Internet Archive (Wayback)
- domain-registered (green), checked 2026-07-28 Domain registry record
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- debarment-clear (green), checked 2026-08-16 OpenSanctions
- sanctions-clear (green), checked 2026-08-16 OpenSanctions
- financials-published (green), checked 2019-12-31 INPI/BCE published accounts (data.economie.gouv.fr)
- export-registered (green), checked 2026-08-30 EU EORI validation (European Commission)
- public-contract-awarded (green), checked 2023-08-04 DECP, French public-procurement register 여기서 낙찰은 남이 한 심사까지 함께 뜻합니다. EU와 EEA에서는 공공 발주자가 사기, 부패, 자금세탁으로 유죄가 확정된 입찰자와 최종 결정으로 세금 또는 사회보험료 체납이 확인된 입찰자를 반드시 배제해야 합니다. Directive 2014/24/EU, Article 57 (exclusion grounds)
- registry-activity (green), checked 2026-08-19 France INSEE Sirene state register (data.gouv.fr bulk file)
- directors-on-file (green), checked 2026-07-09 INSEE Sirene (annuaire-entreprises)
- vat-valid (green), checked 2026-08-05 VIES (European Commission)
- registry-id-verified (green), checked 2026-07-04 Annuaire des Entreprises (INSEE / INPI)
- registry-active-global (green), checked 2026-08-19 France INSEE Sirene state register (data.gouv.fr bulk file)
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)