eudamed_udi Primary ID: D-ABT-CT-A111L9

Accu-Tell® NT-proBNP Strip (Whole Blood/Serum/Plasma) (UDI D-ABT-CT-A111L9)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Accu-Tell® NT-proBNP Strip (Whole Blood/Serum/Plasma) (Model/Catalog Number: ABT-CT-A111) is a medical device manufactured by AccuBioTech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160704 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: ABT-CT-A111
Product Code / EMDN: W0102160704
Device Name: Accu-Tell® NT-proBNP Test
Database Sync Date: 2026-08-09 16:51:51

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® NT-proBNP Strip (Whole Blood/Serum/Plasma)?

The registered manufacturer of record for Accu-Tell® NT-proBNP Strip (Whole Blood/Serum/Plasma) is AccuBioTech Co., Ltd..

What is the Primary UDI-DI identifier for Accu-Tell® NT-proBNP Strip (Whole Blood/Serum/Plasma)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-ABT-CT-A111L9.

What classification code is assigned to this device?

This device is registered under product classification code W0102160704.

Similar Classification Devices (W0102160704)

Other Devices by AccuBioTech Co., Ltd.

Programmatic Export

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

JSON API Endpoint