eudamed_udi Primary ID: 06974439670841

Endoscopic Light Source (UDI 06974439670841)

Manufactured by Nanjing Tuge Healthcare Co., Ltd.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Endoscopic Light Source (Model/Catalog Number: TLS-M821A) is a medical device manufactured by Nanjing Tuge Healthcare Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z12020402 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: TLS-M821A
Product Code / EMDN: Z12020402
Device Name: Endoscopic Light Source
Database Sync Date: 2026-08-09 16:29:01

Full Regulatory Attributes

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{
    "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 Endoscopic Light Source?

The registered manufacturer of record for Endoscopic Light Source is Nanjing Tuge Healthcare Co., Ltd..

What is the Primary UDI-DI identifier for Endoscopic Light Source?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974439670841.

What classification code is assigned to this device?

This device is registered under product classification code Z12020402.

Similar Classification Devices (Z12020402)

Other Devices by Nanjing Tuge Healthcare Co., Ltd.

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