gudid
Primary ID: 28001
AxioGloss (UDI 28001)
Manufactured by Axiodent Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AxioGloss - Primary ID 28001
Device Regulatory Overview
The AxioGloss (Model/Catalog Number: 28001) is a medical device manufactured by Axiodent Inc.. This product is indexed under FDA Product Code / Category Classification EJR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 28001
- Product Code / EMDN
- EJR
- Device Name
- Database Sync Date
- 2026-08-09 09:01:55
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 AxioGloss?
The registered manufacturer of record for AxioGloss is Axiodent Inc..
What is the Primary UDI-DI identifier for AxioGloss?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 28001.
What classification code is assigned to this device?
This device is registered under product classification code EJR.
Similar Classification Devices (EJR)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint