GUDIDData
eudamed_udi Primary ID: 06952804813109

Handheld DOA Reader (UDI 06952804813109)

Manufactured by Assure Tech. (Hangzhou) Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Handheld DOA Reader - Primary ID 06952804813109

Device Regulatory Overview

The Handheld DOA Reader (Model/Catalog Number: ADT3000) is a medical device manufactured by Assure Tech. (Hangzhou) Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0201069099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ADT3000
Product Code / EMDN
W0201069099
Device Name
Handheld DOA Reader
Database Sync Date
2026-08-09 16:48:08

Full Regulatory Attributes

πŸ”’ 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 Handheld DOA Reader?

The registered manufacturer of record for Handheld DOA Reader is Assure Tech. (Hangzhou) Co., Ltd..

What is the Primary UDI-DI identifier for Handheld DOA Reader?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06952804813109.

What classification code is assigned to this device?

This device is registered under product classification code W0201069099.

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