Natus Medical Incorporated
Diagnóstico de neurología y atención neonatal para hospitales de todo el mundo.
Natus Medical es un fabricante de dispositivos y servicios médicos para el diagnóstico y tratamiento de trastornos neurológicos, atención neonatal y discapacidad auditiva. Las líneas de productos incluyen sistemas de monitoreo de EEG, equipos de monitoreo del cerebro de recién nacidos, dispositivos de detección de emisiones otoacústicas y sistemas de fototerapia para la ictericia. Natus presta servicios a departamentos de neurología pediátrica y de adultos en más de 100 países a través de redes de distribuidores y ventas directas.
- Type
- brand seeking distribution
- Location
- Middleton, WI, United States
- Founded
- 1987
- Website
- natus.com
- Categories
- Suministros médicos y sanitarios, Electrónica de consumo
- Markets
- Estados Unidos, Alemania, Reino Unido, Australia, Japón, Brasil
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- manufacturing-practice-certified (green), checked 2026-08-21 ANVISA (Brazilian Health Regulatory Agency), public register of Good Manufacturing Practice certificates (CBPF)
- registered-manufacturer (green), checked 2026-08-21 ALIMS (Medicines and Medical Devices Agency of Serbia), register of medical-device manufacturers
- domain-registered (green), checked 2026-08-09 Domain registry record
- lei-lapsed (amber), checked 2026-08-23 GLEIF global LEI register (golden copy)
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- fda-registered (green), checked 2026-08-09 FDA
- debarment-clear (green), checked 2026-08-09 OpenSanctions
Claimed certifications
- ISO 13485, Medical Devices Quality IAF CertSearch
- CE Marking EU NANDO (notified bodies)
- 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)