gudid
Primary ID: 0-46772
Millennium (UDI 0-46772)
Manufactured by Avalign Technologies, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Millennium - Primary ID 0-46772
Device Regulatory Overview
The Millennium (Model/Catalog Number: 0-46772) is a medical device manufactured by Avalign Technologies, Inc.. This product is indexed under FDA Product Code / Category Classification HTS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0-46772
- Product Code / EMDN
- HTS
- Device Name
- Downing Cartilage Knife, BW 10.5mm OL 266mm (10 1/2")
- Database Sync Date
- 2026-08-09 09:09:24
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 Millennium?
The registered manufacturer of record for Millennium is Avalign Technologies, Inc..
What is the Primary UDI-DI identifier for Millennium?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0-46772.
What classification code is assigned to this device?
This device is registered under product classification code HTS.
Similar Classification Devices (HTS)
Other Devices by Avalign Technologies, Inc.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint