eudamed_udi Primary ID: D-DAL-ACO803NK

Alcohol Rapid Test (UDI D-DAL-ACO803NK)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Alcohol Rapid Test (Model/Catalog Number: DAL-ACO803) is a medical device manufactured by Acro Biotech Inc.. This product is indexed under FDA Product Code / Category Classification W0102160599 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: DAL-ACO803
Product Code / EMDN: W0102160599
Device Name: Alcohol Rapid Test
Database Sync Date: 2026-08-09 16:29:21

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 Alcohol Rapid Test?

The registered manufacturer of record for Alcohol Rapid Test is Acro Biotech Inc..

What is the Primary UDI-DI identifier for Alcohol Rapid Test?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-DAL-ACO803NK.

What classification code is assigned to this device?

This device is registered under product classification code W0102160599.

Similar Classification Devices (W0102160599)

Other Devices by Acro Biotech Inc.

Programmatic Export

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

JSON API Endpoint