gudid
Primary ID: VM104-9166
Avalign (UDI VM104-9166)
Manufactured by Avalign Technologies, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Avalign - Primary ID VM104-9166
Device Regulatory Overview
The Avalign (Model/Catalog Number: VM104-9166) is a medical device manufactured by Avalign Technologies, Inc.. This product is indexed under FDA Product Code / Category Classification JZF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VM104-9166
- Product Code / EMDN
- JZF
- Device Name
- Ferguson Frazier Suction Tube,
- Database Sync Date
- 2026-08-09 09:02:38
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 Avalign?
The registered manufacturer of record for Avalign is Avalign Technologies, Inc..
What is the Primary UDI-DI identifier for Avalign?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VM104-9166.
What classification code is assigned to this device?
This device is registered under product classification code JZF.
Similar Classification Devices (JZF)
Other Devices by Avalign Technologies, Inc.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint