gudid Primary ID: D8 LED

DTE (UDI D8 LED)

Manufactured by Guilin Woodpecker Medical Instrument Co., Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The DTE (Model/Catalog Number: D8 LED) is a medical device manufactured by Guilin Woodpecker Medical Instrument Co., Ltd.. This product is indexed under FDA Product Code / Category Classification ELC within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: D8 LED
Product Code / EMDN: ELC
Device Name: Ultrasonic Scaler
Database Sync Date: 2026-08-09 09:11:05

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 DTE?

The registered manufacturer of record for DTE is Guilin Woodpecker Medical Instrument Co., Ltd..

What is the Primary UDI-DI identifier for DTE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D8 LED.

What classification code is assigned to this device?

This device is registered under product classification code ELC.

Similar Classification Devices (ELC)

Other Devices by Guilin Woodpecker Medical Instrument Co., Ltd.

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