Manufacturer profileFisher & Paykel Healthcare Ltd
Manufacturer • New Zealand260 devices on the TGA ARTG5 device classesApr 06, 2004 – Dec 18, 2024
VerifiedTGA · Australian Register of Therapeutic Goods
260
Total devices
5
Device classes
2004
Earliest registration
2024
Latest registration
Regulatory footprint
Search Fisher & Paykel Healthcare Ltd across other regulatory registries
Thailand
European Union
Colombia
South Korea
Canada
EcuadorRecent device registrations
Latest 10 TGA ARTG device registrations
Humidified oxygen administration set
ARTG 473715Sponsor: Fisher & Paykel Healthcare Pty Ltd
Class IIb · Dec 18, 2024
Humidified oxygen administration set
ARTG 473715Sponsor: Fisher & Paykel Healthcare Pty Ltd
Class IIb · Dec 18, 2024
Oesophageal intubation detector, exhaled carbon dioxide, adult
ARTG 463405Sponsor: Fisher & Paykel Healthcare Pty Ltd
Class I · Oct 02, 2024
Oxygen low pressure tubing
ARTG 462155Sponsor: Fisher & Paykel Healthcare Pty Ltd
Class IIa · Sep 11, 2024
Home CPAP unit
Sponsor: Fisher & Paykel Healthcare Pty Ltd
Class IIa · Mar 07, 2024
Home CPAP unit
ARTG 443370Sponsor: Fisher & Paykel Healthcare Pty Ltd
Class IIa · Mar 07, 2024
CPAP/BiPAP face mask, single-use
Sponsor: Fisher & Paykel Healthcare Pty Ltd
Class IIb · Jan 17, 2024
CPAP/BiPAP face mask, single-use
ARTG 434550Sponsor: Fisher & Paykel Healthcare Pty Ltd
Class IIb · Jan 17, 2024
Inspiratory line humidification chamber, single-use
ARTG 421901Sponsor: Fisher & Paykel Healthcare Pty Ltd
Class IIa · Sep 15, 2023
Inspiratory line humidification chamber, single-use
Sponsor: Fisher & Paykel Healthcare Pty Ltd
Class IIa · Sep 15, 2023
Risk class distribution
Devices by risk class
Class I9536.5% of total
Class IIa12347.3% of total
Class IIb3814.6% of total
Class Is20.8% of total
Class Im20.8% of total
About this profile
Explore comprehensive manufacturer profile for Fisher & Paykel Healthcare Ltd through Pure Global AI's free Australia TGA ARTG medical device database. This company has manufactured 260 medical devices registered with TGA ARTG across 5 device classes. This manufacturer is based in New Zealand. Their registration history spans from Apr 06, 2004 to Dec 18, 2024.
This page provides detailed insights including recent device registrations, risk class distribution (Class IIa: 123, Class I: 95, Class IIb: 38, Class Im: 2, Class Is: 2), and complete regulatory information from the official Australia TGA ARTG medical device database. Pure Global AI offers free access to Australia's medical device registry with 62k records.