GUDIDData
gudid Primary ID: D-T1002

IPL Home Use Hair Removal Device (UDI D-T1002)

Manufactured by Dongguan Letme Medical Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IPL Home Use Hair Removal Device - Primary ID D-T1002

Device Regulatory Overview

The IPL Home Use Hair Removal Device (Model/Catalog Number: D-T1002) is a medical device manufactured by Dongguan Letme Medical Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification OHT within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
D-T1002
Product Code / EMDN
OHT
Device Name
IPL Home Use Hair Removal Device
Database Sync Date
2026-08-09 09:06:36

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 IPL Home Use Hair Removal Device?

The registered manufacturer of record for IPL Home Use Hair Removal Device is Dongguan Letme Medical Technology Co., Ltd..

What is the Primary UDI-DI identifier for IPL Home Use Hair Removal Device?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-T1002.

What classification code is assigned to this device?

This device is registered under product classification code OHT.

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