gudid Primary ID: VM106-0242

Avalign (UDI VM106-0242)

Manufactured by Avalign Technologies, Inc.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Avalign (Model/Catalog Number: VM106-0242) is a medical device manufactured by Avalign Technologies, Inc.. This product is indexed under FDA Product Code / Category Classification KAK within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: VM106-0242
Product Code / EMDN: KAK
Device Name: Probe Right Angle
Database Sync Date: 2026-08-09 09:02:38

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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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 VM106-0242.

What classification code is assigned to this device?

This device is registered under product classification code KAK.

Similar Classification Devices (KAK)

Other Devices by Avalign Technologies, Inc.

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