gudid
Primary ID: 7
Nodify Lung (PR) (UDI 7)
Manufactured by Biodesix, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Nodify Lung (PR) - Primary ID 7
Device Regulatory Overview
The Nodify Lung (PR) (Model/Catalog Number: 7) is a medical device manufactured by Biodesix, Inc.. This product is indexed under FDA Product Code / Category Classification PQD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7
- Product Code / EMDN
- PQD
- Device Name
- Sample Collection Kit
- Database Sync Date
- 2026-08-09 09:03:56
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 Nodify Lung (PR)?
The registered manufacturer of record for Nodify Lung (PR) is Biodesix, Inc..
What is the Primary UDI-DI identifier for Nodify Lung (PR)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 7.
What classification code is assigned to this device?
This device is registered under product classification code PQD.
Similar Classification Devices (PQD)
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