ResMed
Apnea del sueño, cuidados respiratorios y dispositivos sanitarios conectados.
ResMed fabrica dispositivos para la apnea del sueño, atención respiratoria y dispositivos de salud conectados desde sus operaciones en Sydney. La empresa suministra sistemas de atención médica, laboratorios, socios OEM o clientes de exportación regulados en sus mercados primarios listados.
- Type
- brand seeking distribution
- Location
- Sydney, Australia
- Founded
- 1989
- Website
- resmed.com
- Categories
- Suministros médicos y sanitarios, Wearables y dispositivos personales
- Markets
- Australia, Estados Unidos, Alemania, Japón
Verified facts
- customer-reviews (amber), checked 2026-08-12 ProductReview.com.au
- domain-registered (green), checked 2026-08-12 Domain registry record
- sanctions-clear (green), checked 2026-08-12 OpenSanctions
- debarment-clear (green), checked 2026-08-12 OpenSanctions
- fda-registered (green), checked 2026-08-12 FDA
Claimed certifications
- ISO 13485, Medical Devices Quality IAF CertSearch
- FDA Registered FDA Establishment Registration
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)
- Electronics for the EU need CE marking incl. RoHS substance limits, and producers must register for WEEE take-back in each member state of sale. European Commission (CE)
- Electronics for the US market need FCC equipment authorization under 47 CFR Part 15, which covers unintentional radiators such as switch-mode power supplies, not only radio devices. US FCC (Part 15)