Fisher & Paykel Healthcare
Fisher & Paykel Healthcare fabrique des appareils de soins respiratoires pour les canaux B2B prêts à l'exportation.
Fisher & Paykel Healthcare fabrique des appareils de soins respiratoires, des systèmes d'humidification, des masques et du matériel hospitalier à Auckland. Fondée en 1969, la société fournit des hôpitaux, des cliniques, des distributeurs médicaux et des marchés d'exportation réglementés en Nouvelle-Zélande, en Australie, aux États-Unis, en Grande-Bretagne et sur les marchés d'exportation associés.
- Type
- brand seeking distribution
- Location
- Auckland, New Zealand
- Founded
- 1969
- Website
- fphcare.com
- Categories
- Fournitures médicales et de santé
- Markets
- Nouvelle-Zélande, Australie, États-Unis, Royaume-Uni
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)