gudid Primary ID: 29601002

JMU (UDI 29601002)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The JMU (Model/Catalog Number: 29601002) is a medical device manufactured by JMU DENTAL, INC. This product is indexed under FDA Product Code / Category Classification GBX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 29601002
Product Code / EMDN: GBX
Device Name: JMU Disposable Dental Implant Irrigation Tubing, W&H Type, EO Gas Sterilized, 1pc/bag, 300pcs/case - Recommended for use on W&H implant devices
Database Sync Date: 2026-08-09 09:01:13

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 JMU?

The registered manufacturer of record for JMU is JMU DENTAL, INC.

What is the Primary UDI-DI identifier for JMU?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 29601002.

What classification code is assigned to this device?

This device is registered under product classification code GBX.

Similar Classification Devices (GBX)

Other Devices by JMU DENTAL, INC

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