eudamed_udi
Primary ID: 04712568360491
NasalSpec (UDI 04712568360491)
Manufactured by NORTH EOS INDUSTRIES,INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NasalSpec - Primary ID 04712568360491
Device Regulatory Overview
The NasalSpec (Model/Catalog Number: NasalSpec-Mini(1)) is a medical device manufactured by NORTH EOS INDUSTRIES,INC.. This product is indexed under FDA Product Code / Category Classification L149004 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NasalSpec-Mini(1)
- Product Code / EMDN
- L149004
- Device Name
- NasalSpec
- Database Sync Date
- 2026-08-09 16:29:14
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 NasalSpec?
The registered manufacturer of record for NasalSpec is NORTH EOS INDUSTRIES,INC..
What is the Primary UDI-DI identifier for NasalSpec?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04712568360491.
What classification code is assigned to this device?
This device is registered under product classification code L149004.
Similar Classification Devices (L149004)
Other Devices by NORTH EOS INDUSTRIES,INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint