GUDIDData
eudamed_udi Primary ID: D1231001450

KOPP ELEVATOR UPPER (UDI D1231001450)

Manufactured by Dental Expert

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KOPP ELEVATOR UPPER - Primary ID D1231001450

Device Regulatory Overview

The KOPP ELEVATOR UPPER (Model/Catalog Number: 1001-45) is a medical device manufactured by Dental Expert. This product is indexed under FDA Product Code / Category Classification Q010399 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1001-45
Product Code / EMDN
Q010399
Device Name
KOPP ELEVATOR UPPER
Database Sync Date
2026-08-09 16:28:57

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 KOPP ELEVATOR UPPER?

The registered manufacturer of record for KOPP ELEVATOR UPPER is Dental Expert.

What is the Primary UDI-DI identifier for KOPP ELEVATOR UPPER?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D1231001450.

What classification code is assigned to this device?

This device is registered under product classification code Q010399.

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