gudid
Primary ID: Aladdin
Aladdin (UDI Aladdin)
Manufactured by DXM CO., LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Aladdin - Primary ID Aladdin
Device Regulatory Overview
The Aladdin (Model/Catalog Number: Aladdin) is a medical device manufactured by DXM CO., LTD. This product is indexed under FDA Product Code / Category Classification EEG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Aladdin
- Product Code / EMDN
- EEG
- Device Name
- This visible ray curing light is a device to enhance a bleaching effect by exposing a visible ray to teeth with a bleaching agent is designed to be used in dental clinics.This device emits 440 - 50nm blue visible ray by using 3 pieces of L.E.D (Light-Emitting Diode). It is a wireless type device and is convenient to move inside of the clinic..Aladdin features are:- Easy to operate with touch switches to control the light intensity or operation time.- Easy to carry or move. Once charged, the power code is not necessary to keep plugged in during operation.- Removable parts like head, recharging unit, adapter, pole & foot.- Adjustable light intensity. Left, Center & Right LEDs have 3 grades of light intensity (High, Normal & Low).- Easy to store.
- Database Sync Date
- 2026-08-09 09:28:56
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Aladdin?
The registered manufacturer of record for Aladdin is DXM CO., LTD.
What is the Primary UDI-DI identifier for Aladdin?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Aladdin.
What classification code is assigned to this device?
This device is registered under product classification code EEG.
Similar Classification Devices (EEG)
Other Devices by DXM CO., LTD
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