LIFEAZ (LIFE)
Join more than 25,000 equipped families and businesses. Connected defibrillator, maintenance included, training in life-saving actions.
Join more than 25,000 equipped families and businesses. Connected defibrillator, maintenance included, training in life-saving actions.
- Type
- Manufacturer
- Location
- Paris, France
- Founded
- 2015
- Website
- https://www.lifeaz.co
- Categories
- Medical & Healthcare Supplies
Listed in a source registry
France INSEE Sirene / INPI RNE state register (annuaire-entreprises.data.gouv.fr)
Verified facts
- web-presence-since (green), checked 2026-08-20 Internet Archive (Wayback)
- sanctions-clear (green), checked 2026-08-03 OpenSanctions
- vat-valid (green), checked 2026-08-03 VIES
- debarment-clear (green), checked 2026-08-03 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-03 Mail server of the company domain
- registered-since (green), checked 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- public-contract-awarded (green), checked 2024-06-26 DECP, French public-procurement register Here the award carries someone else's check: in the EU and the EEA a public buyer must exclude bidders convicted of fraud, corruption or money laundering, and those found by a final decision to owe taxes or social contributions. Directive 2014/24/EU, Article 57 (exclusion grounds)
- bodacc-accounts-filed (green), checked 2026-08-03 BODACC (annuaire-entreprises)
- directors-on-file (green), checked 2026-08-03 INSEE Sirene (annuaire-entreprises)
- registry-active-global (green), checked 2026-08-19 France INSEE Sirene state register (data.gouv.fr bulk file)
- registry-id-verified (green), checked 2026-07-22 Annuaire des Entreprises (INSEE / INPI)
- workforce-on-record (green), checked 2026-07-01 INSEE SIRENE (Registre national des entreprises)
- registered-manufacturer (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)