GUDIDData
eudamed_udi Primary ID: 00810036780179

Julius Wirth (UDI 00810036780179)

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 00810036780179

Device Regulatory Overview

The Julius Wirth (Model/Catalog Number: 102-009) is a medical device manufactured by J&J Instruments, LLC. This product is indexed under FDA Product Code / Category Classification L159003 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
102-009
Product Code / EMDN
L159003
Device Name
Dental Device
Database Sync Date
2026-08-09 16:58:54

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

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 00810036780179.

What classification code is assigned to this device?

This device is registered under product classification code L159003.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint