gudid Primary ID: VM37-2313

Avalign (UDI VM37-2313)

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: VM37-2313) is a medical device manufactured by Avalign Technologies, Inc.. This product is indexed under FDA Product Code / Category Classification HTX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: VM37-2313
Product Code / EMDN: HTX
Device Name: Leksell Rongeur, curved
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 VM37-2313.

What classification code is assigned to this device?

This device is registered under product classification code HTX.

Similar Classification Devices (HTX)

Other Devices by Avalign Technologies, Inc.

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