Fisher & Paykel Healthcare
Fisher & Paykel Healthcare stellt Beatmungsgeräte für exportfähige B2B-Kanäle her.
Fisher & Paykel Healthcare stellt in Auckland Beatmungsgeräte, Befeuchtungssysteme, Masken und Krankenhausausrüstung her. Das 1969 gegründete Unternehmen beliefert Krankenhäuser, Kliniken, medizinische Händler und regulierte Exportmärkte in Neuseeland, Australien, den USA, Großbritannien und verwandten Exportmärkten.
- Type
- brand seeking distribution
- Location
- Auckland, New Zealand
- Founded
- 1969
- Website
- fphcare.com
- Categories
- Medizin- & Gesundheitsbedarf
- Markets
- Neuseeland, Australien, Vereinigte Staaten, Vereinigtes Königreich
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)