eudamed_udi
Primary ID: +B99893699990588901/$AN-711220130725+
AirPhysio (UDI +B99893699990588901/$AN-711220130725+)
Manufactured by AirPhysio Pty Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AirPhysio - Primary ID +B99893699990588901/$AN-711220130725+
Device Regulatory Overview
The AirPhysio (Model/Catalog Number: 9369998021505) is a medical device manufactured by AirPhysio Pty Ltd. This product is indexed under FDA Product Code / Category Classification R900902 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9369998021505
- Product Code / EMDN
- R900902
- Device Name
- AirPhysio OPEP Device
- Database Sync Date
- 2026-08-09 17:13:28
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of AirPhysio?
The registered manufacturer of record for AirPhysio is AirPhysio Pty Ltd.
What is the Primary UDI-DI identifier for AirPhysio?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +B99893699990588901/$AN-711220130725+.
What classification code is assigned to this device?
This device is registered under product classification code R900902.
Similar Classification Devices (R900902)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint