Masimo
Hasta izleme, nabız oksimetresi ve hastane otomasyon cihazları.
Masimo, Irvine operasyonlarından hasta izleme, nabız oksimetresi ve hastane otomasyon cihazları üretmektedir. Şirket, listelenen birincil pazarlarda sağlık sistemleri, laboratuvarlar, OEM ortakları veya düzenlemeye tabi ihracat müşterilerine hizmet vermektedir.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Irvine, United States
- Founded
- 1989
- Website
- masimo.com
- Categories
- Tıbbi ve Sağlık Malzemeleri, Giyilebilir Ürünler ve Kişisel Cihazlar
- Markets
- Amerika Birleşik Devletleri, Almanya, Japonya, Avustralya
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 2026-08-07 Domain registry record
- facility-registered (green), checked 2026-08-07 US EPA Facility Registry Service (national combined file)
- registered-manufacturer (green), checked 2026-08-21 ALIMS (Medicines and Medical Devices Agency of Serbia), register of medical-device manufacturers
- lei-active (green), checked 2026-09-07 GLEIF global LEI register (golden copy)
- places-goods-on-market (green), checked 2026-09-07 Registre national des producteurs (ADEME/SYDEREP), France
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
Claimed certifications, not confirmed by us
- 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)