GUDIDData
eudamed_udi Primary ID: 06970581430715

Accu-Tell® Urine Reagent Strips 2Para (UDI 06970581430715)

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® Urine Reagent Strips 2Para - Primary ID 06970581430715

Device Regulatory Overview

The Accu-Tell® Urine Reagent Strips 2Para (Model/Catalog Number: ABT-UM-A334) is a medical device manufactured by AccuBioTech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0101060204 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ABT-UM-A334
Product Code / EMDN
W0101060204
Device Name
Accu-Tell® Urine Reagent Strips
Database Sync Date
2026-08-09 16:48:46

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® Urine Reagent Strips 2Para?

The registered manufacturer of record for Accu-Tell® Urine Reagent Strips 2Para is AccuBioTech Co., Ltd..

What is the Primary UDI-DI identifier for Accu-Tell® Urine Reagent Strips 2Para?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06970581430715.

What classification code is assigned to this device?

This device is registered under product classification code W0101060204.

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