GUDIDData
eudamed_udi Primary ID: D1231017130

BURNISHER EXPLORER 1.15mm/1.75mm (UDI D1231017130)

Manufactured by Dental Expert

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BURNISHER EXPLORER 1.15mm/1.75mm - Primary ID D1231017130

Device Regulatory Overview

The BURNISHER EXPLORER 1.15mm/1.75mm (Model/Catalog Number: 1017-13) is a medical device manufactured by Dental Expert. This product is indexed under FDA Product Code / Category Classification L159003 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1017-13
Product Code / EMDN
L159003
Device Name
EXPLORER 1.15mm/1.75mm
Database Sync Date
2026-08-09 16:30:27

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 BURNISHER EXPLORER 1.15mm/1.75mm?

The registered manufacturer of record for BURNISHER EXPLORER 1.15mm/1.75mm is Dental Expert.

What is the Primary UDI-DI identifier for BURNISHER EXPLORER 1.15mm/1.75mm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D1231017130.

What classification code is assigned to this device?

This device is registered under product classification code L159003.

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