iRhythm Technologies
Dispositifs médicaux, fournitures de soins de santé et produits cliniques.
iRhythm Technologies fabrique des dispositifs médicaux, des fournitures de soins de santé et des produits cliniques à partir de ses opérations de San Francisco. La société fournit des acheteurs d'hôpitaux, des distributeurs cliniques, des systèmes de santé ou des clients exportateurs sur ses principaux marchés cotés.
- Type
- brand seeking distribution
- Location
- San Francisco, United States
- Founded
- 2006
- Website
- irhythmtech.com
- Categories
- Fournitures médicales et de santé, Fournitures industrielles
- Markets
- États-Unis, Allemagne, Japon, Brésil
Verified facts
- certificate-page-on-site (amber), checked 2026-08-11 Company's own certification page
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- domain-registered (green), checked 2026-08-08 Domain registry record
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- facility-registered (green), checked 2026-08-07 US EPA Facility Registry Service (national combined file)
- registry-id-verified (green), checked 2026-08-13 California Secretary of State (bizfile Online)
- registry-active-global (green), checked 2026-08-13 California Secretary of State (bizfile Online)
- registered-since (green), checked 2026-08-13 California Secretary of State (bizfile Online)
Claimed certifications
- ISO 13485, Medical Devices Quality IAF CertSearch
- CE Marking EU NANDO (notified bodies)
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)