gudid Primary ID: 3.2

Quentry.com (Quentry Web) Quentry Gateway Quentry Desktop (UDI 3.2)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Quentry.com (Quentry Web) Quentry Gateway Quentry Desktop (Model/Catalog Number: 3.2) is a medical device manufactured by Brainlab SE. This product is indexed under FDA Product Code / Category Classification LMD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 3.2
Product Code / EMDN: LMD
Device Name
Database Sync Date: 2026-08-09 09:26:08

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 Quentry.com (Quentry Web) Quentry Gateway Quentry Desktop?

The registered manufacturer of record for Quentry.com (Quentry Web) Quentry Gateway Quentry Desktop is Brainlab SE.

What is the Primary UDI-DI identifier for Quentry.com (Quentry Web) Quentry Gateway Quentry Desktop?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3.2.

What classification code is assigned to this device?

This device is registered under product classification code LMD.

Similar Classification Devices (LMD)

Other Devices by Brainlab SE

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