gudid Primary ID: G2033A

Garg (UDI G2033A)

Manufactured by Power Dental U.S.A. Inc.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Garg (Model/Catalog Number: G2033A) is a medical device manufactured by Power Dental U.S.A. Inc.. This product is indexed under FDA Product Code / Category Classification MDM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: G2033A
Product Code / EMDN: MDM
Device Name: BONE GRAFT PACKER 1.0 / 1.4 mm (8-11-13-15-18 mm) TITANIUM
Database Sync Date: 2026-08-09 09:01:11

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 Garg?

The registered manufacturer of record for Garg is Power Dental U.S.A. Inc..

What is the Primary UDI-DI identifier for Garg?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G2033A.

What classification code is assigned to this device?

This device is registered under product classification code MDM.

Similar Classification Devices (MDM)

Other Devices by Power Dental U.S.A. Inc.

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