LABORATOIRES URGO (URGO MEDICAL - MDFA (MEDICAL DEVICE FOR ALL))
Produkcja farmaceutyczna, Francja
LABORATOIRES URGO (URGO MEDICAL - MDFA (URZĄDZENIE MEDYCZNE DLA WSZYSTKICH)) to firma farmaceutyczna z siedzibą w Chenove we Francji.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Chenove, France
- Founded
- 2000
- Website
- http://www.urgo.fr
- Categories
- Produkcja farmaceutyczna
Listed in a source registry
France INSEE Sirene / INPI RNE state register (annuaire-entreprises.data.gouv.fr)
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- domain-registered (green), checked 2026-07-28 Domain registry record
- facility-inspected (green), checked 2026-08-20 Georisques, French register of classified installations (ICPE)
- workforce-on-record (green), effective since 2026-07-01 INSEE SIRENE (Registre national des entreprises)
- registered-since (green), effective since 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- web-presence-since (green), checked 2026-08-21 Internet Archive (Wayback)
- debarment-clear (green), checked 2026-08-16 OpenSanctions
- sanctions-clear (green), checked 2026-08-16 OpenSanctions
- places-goods-on-market (green), checked 2026-09-07 Registre national des producteurs (ADEME/SYDEREP), France
- public-contract-awarded (green), effective since 2026-06-26 TED (Tenders Electronic Daily), EU public procurement award notices Tutaj wygrana niesie też cudzą kontrolę: w UE i EOG zamawiający musi wykluczyć wykonawcę skazanego za oszustwo, korupcję lub pranie pieniędzy oraz takiego, wobec którego prawomocnie stwierdzono zaległości podatkowe lub składkowe. Directive 2014/24/EU, Article 57 (exclusion grounds)
- financials-published (green), effective since 2019-12-31 INPI/BCE published accounts (data.economie.gouv.fr)
- registry-activity (green), checked 2026-09-07 France INSEE Sirene state register (data.gouv.fr bulk file)
- industrial-site-registered (green), effective since 2024-12-31 IREP, French register of pollutant releases and waste (declared by the operator)
- facility-activity-described (green), checked 2026-08-20 Georisques, French register of classified installations (ICPE)
- operating-permit (green), effective since 2026-04-28 Georisques, French register of classified installations (ICPE)
- registered-manufacturer (green), checked 2026-09-17 Ministero della Salute, banca dati e Repertorio dei dispositivi medici
- directors-on-file (green), checked 2026-07-09 INSEE Sirene (annuaire-entreprises)
- registry-active-global (green), checked 2026-09-07 France INSEE Sirene state register (data.gouv.fr bulk file)
- registered-address (green), checked 2026-08-10 INSEE Sirene (annuaire-entreprises)
- vat-valid (green), checked 2026-08-05 VIES (European Commission)
- export-registered (green), checked 2026-09-21 EU EORI validation (European Commission)
Import rules for these goods
- Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)