GUDIDData
eudamed_udi Primary ID: 04719872332459

Van Lent Systems (UDI 04719872332459)

Manufactured by ZMI Electronics Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Van Lent Systems - Primary ID 04719872332459

Device Regulatory Overview

The Van Lent Systems (Model/Catalog Number: PRU-050090-VLS) is a medical device manufactured by ZMI Electronics Ltd.. This product is indexed under FDA Product Code / Category Classification Z120601 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
PRU-050090-VLS
Product Code / EMDN
Z120601
Device Name
Rubber Electrode
Database Sync Date
2026-08-09 16:28:53

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 Van Lent Systems?

The registered manufacturer of record for Van Lent Systems is ZMI Electronics Ltd..

What is the Primary UDI-DI identifier for Van Lent Systems?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04719872332459.

What classification code is assigned to this device?

This device is registered under product classification code Z120601.

Programmatic Export

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

JSON API Endpoint