GUDIDData
gudid Primary ID: 3738-930

Z3 (UDI 3738-930)

Manufactured by BENCO DENTAL SUPPLY CO.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Z3 - Primary ID 3738-930

Device Regulatory Overview

The Z3 (Model/Catalog Number: 3738-930) is a medical device manufactured by BENCO DENTAL SUPPLY CO.. This product is indexed under FDA Product Code / Category Classification MED within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
3738-930
Product Code / EMDN
MED
Device Name
Benco Z3 3.4% 30 DAY GLUT
Database Sync Date
2026-08-09 09:20:07

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 Z3?

The registered manufacturer of record for Z3 is BENCO DENTAL SUPPLY CO..

What is the Primary UDI-DI identifier for Z3?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3738-930.

What classification code is assigned to this device?

This device is registered under product classification code MED.

Programmatic Export

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

JSON API Endpoint