Fisher & Paykel Healthcare
Fisher & Paykel Healthcare производит устройства респираторной терапии для экспортных каналов B2B.
Fisher & Paykel Healthcare производит устройства для ухода за органами дыхания, системы увлажнения, маски и больничное оборудование в Окленде. Основанная в 1969 году, компания снабжает больницы, клиники, дистрибьюторов медицинских товаров и регулируемые экспортные рынки Новой Зеландии, Австралии, США, Великобритании и связанных с ними экспортных рынков.
- Type
- brand seeking distribution
- Location
- Auckland, New Zealand
- Founded
- 1969
- Website
- fphcare.com
- Categories
- Медицинские товары и расходники
- Markets
- Новая Зеландия, Австралия, Соединенные Штаты, Великобритания
Verified facts
- 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
- fda-registered (green), checked 2026-08-08 FDA
- lei-active (green), checked 2026-08-08 GLEIF
- registry-id-verified (green), checked 2026-08-21 Companies Register (NZBN bulk data)
- registry-active-global (green), checked 2026-08-21 New Zealand Companies Office (NZBN bulk data)
- registered-since (green), checked 2026-08-21 New Zealand Companies Office (NZBN bulk data)
- directors-on-file (green), checked 2026-08-21 New Zealand Companies Office (NZBN bulk data)
- registered-manufacturer (green), checked 2026-08-22 Agencia Estatal de Medicamentos y Tecnologias en Salud (AGEMED, Bolivia), listado oficial de registros sanitarios aprobados
Claimed certifications
- 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)