eudamed_udi
Primary ID: 09420012469755
F&P AIRVO 3 (UDI 09420012469755)
Manufactured by Fisher & Paykel Healthcare Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for F&P AIRVO 3 - Primary ID 09420012469755
Device Regulatory Overview
The F&P AIRVO 3 (Model/Catalog Number: PT301EW) is a medical device manufactured by Fisher & Paykel Healthcare Limited. This product is indexed under FDA Product Code / Category Classification Z1203010504 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PT301EW
- Product Code / EMDN
- Z1203010504
- Device Name
- Respiratory Support Device
- Database Sync Date
- 2026-08-09 16:29:26
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of F&P AIRVO 3?
The registered manufacturer of record for F&P AIRVO 3 is Fisher & Paykel Healthcare Limited.
What is the Primary UDI-DI identifier for F&P AIRVO 3?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09420012469755.
What classification code is assigned to this device?
This device is registered under product classification code Z1203010504.
Similar Classification Devices (Z1203010504)
Other Devices by Fisher & Paykel Healthcare Limited
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