pma
Primary ID: P200044
LungFit PH (UDI P200044)
Manufactured by Beyond Air, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LungFit PH - Primary ID P200044
Device Regulatory Overview
The LungFit PH (Model/Catalog Number: Unspecified) is a medical device manufactured by Beyond Air, Inc.. This product is indexed under FDA Product Code / Category Classification QTB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- QTB
- Device Name
- Nitric Oxide Generator and Delivery System
- Database Sync Date
- 2026-08-09 10:04:50
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 LungFit PH?
The registered manufacturer of record for LungFit PH is Beyond Air, Inc..
What is the Primary UDI-DI identifier for LungFit PH?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P200044.
What classification code is assigned to this device?
This device is registered under product classification code QTB.
Similar Classification Devices (QTB)
Other Devices by Beyond Air, Inc.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint