GUDIDData
eudamed_udi Primary ID: 06942512502624

NiTi Super Files Gold (UDI 06942512502624)

Manufactured by Shenzhen Denco Medical Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NiTi Super Files Gold - Primary ID 06942512502624

Device Regulatory Overview

The NiTi Super Files Gold (Model/Catalog Number: CODE0121S1) is a medical device manufactured by Shenzhen Denco Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Q010507 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
CODE0121S1
Product Code / EMDN
Q010507
Device Name
Dental Root Canal Instruments Files
Database Sync Date
2026-08-09 16:28:50

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 NiTi Super Files Gold?

The registered manufacturer of record for NiTi Super Files Gold is Shenzhen Denco Medical Co., Ltd..

What is the Primary UDI-DI identifier for NiTi Super Files Gold?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06942512502624.

What classification code is assigned to this device?

This device is registered under product classification code Q010507.

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