GUDIDData
eudamed_udi Primary ID: 00810036780742

Julius Wirth (UDI 00810036780742)

Manufactured by J&J Instruments, LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Julius Wirth - Primary ID 00810036780742

Device Regulatory Overview

The Julius Wirth (Model/Catalog Number: 203-013) is a medical device manufactured by J&J Instruments, LLC. This product is indexed under FDA Product Code / Category Classification L159012 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
203-013
Product Code / EMDN
L159012
Device Name
Dental Device
Database Sync Date
2026-08-09 16:48:16

Full Regulatory Attributes

🔒 Token Gated
{
    "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 Julius Wirth?

The registered manufacturer of record for Julius Wirth is J&J Instruments, LLC.

What is the Primary UDI-DI identifier for Julius Wirth?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00810036780742.

What classification code is assigned to this device?

This device is registered under product classification code L159012.

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