gudid Primary ID: 006-RES

Resilien Moldable (UDI 006-RES)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Resilien Moldable (Model/Catalog Number: 006-RES) is a medical device manufactured by Biogennix, LLC. This product is indexed under FDA Product Code / Category Classification MQV within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 006-RES
Product Code / EMDN: MQV
Device Name: Resilien Moldable 6cc
Database Sync Date: 2026-08-09 09:43:40

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 Resilien Moldable?

The registered manufacturer of record for Resilien Moldable is Biogennix, LLC.

What is the Primary UDI-DI identifier for Resilien Moldable?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 006-RES.

What classification code is assigned to this device?

This device is registered under product classification code MQV.

Similar Classification Devices (MQV)

Other Devices by Biogennix, LLC

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