GUDIDData
eudamed_udi Primary ID: D-ABT-DOA-N340SX

Accu-Tell® Multi-2 Drug Cup W/Indicator (Saliva) (UDI D-ABT-DOA-N340SX)

Manufactured by AccuBioTech Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Accu-Tell® Multi-2 Drug Cup W/Indicator (Saliva) - Primary ID D-ABT-DOA-N340SX

Device Regulatory Overview

The Accu-Tell® Multi-2 Drug Cup W/Indicator (Saliva) (Model/Catalog Number: ABT-DOA-N340) is a medical device manufactured by AccuBioTech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160511 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ABT-DOA-N340
Product Code / EMDN
W0102160511
Device Name
Accu-Tell® Multi-2 Drug Cup W/Indicator (Saliva)
Database Sync Date
2026-08-09 16:28:47

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 Accu-Tell® Multi-2 Drug Cup W/Indicator (Saliva)?

The registered manufacturer of record for Accu-Tell® Multi-2 Drug Cup W/Indicator (Saliva) is AccuBioTech Co., Ltd..

What is the Primary UDI-DI identifier for Accu-Tell® Multi-2 Drug Cup W/Indicator (Saliva)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-ABT-DOA-N340SX.

What classification code is assigned to this device?

This device is registered under product classification code W0102160511.

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