gudid
Primary ID: 72-5225539B3
Millennium (UDI 72-5225539B3)
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 72-5225539B3
Device Regulatory Overview
The Millennium (Model/Catalog Number: 72-5225539B3) is a medical device manufactured by Avalign Technologies, Inc.. This product is indexed under FDA Product Code / Category Classification GCJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 72-5225539B3
- Product Code / EMDN
- GCJ
- Device Name
- 5mm 33cm Fenestrated Grasper, 20mm double action jaw, rotatable 1-piece with flush port, type 3 handle: non-insulated stainless steel
- Database Sync Date
- 2026-08-09 09:02:35
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 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 72-5225539B3.
What classification code is assigned to this device?
This device is registered under product classification code GCJ.
Similar Classification Devices (GCJ)
Other Devices by Avalign Technologies, Inc.
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