GUDIDData
eudamed_udi Primary ID: 06970581431774

Accu-Tell® COT Cassette (Urine) (UDI 06970581431774)

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® COT Cassette (Urine) - Primary ID 06970581431774

Device Regulatory Overview

The Accu-Tell® COT Cassette (Urine) (Model/Catalog Number: ABT-DOA-B141) is a medical device manufactured by AccuBioTech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160599 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ABT-DOA-B141
Product Code / EMDN
W0102160599
Device Name
Accu-Tell® COT Test
Database Sync Date
2026-08-09 16:50:55

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Accu-Tell® COT Cassette (Urine)?

The registered manufacturer of record for Accu-Tell® COT Cassette (Urine) is AccuBioTech Co., Ltd..

What is the Primary UDI-DI identifier for Accu-Tell® COT Cassette (Urine)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06970581431774.

What classification code is assigned to this device?

This device is registered under product classification code W0102160599.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint