Fisher & Paykel Healthcare
Fisher & Paykel Healthcare fabrica dispositivos para el cuidado respiratorio para canales B2B listos para la exportación.
Fisher & Paykel Healthcare fabrica dispositivos para el cuidado respiratorio, sistemas de humidificación, mascarillas y equipos hospitalarios en Auckland. Fundada en 1969, la empresa suministra a hospitales, clínicas, distribuidores médicos y mercados de exportación regulados en Nueva Zelanda, Australia, EE. UU., Gran Bretaña y mercados de exportación relacionados.
- Type
- brand seeking distribution
- Location
- Auckland, New Zealand
- Founded
- 1969
- Website
- fphcare.com
- Categories
- Suministros médicos y sanitarios
- Markets
- Nueva Zelanda, Australia, Estados Unidos, Reino Unido
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)