GUDIDData
eudamed_udi Primary ID: 05700573002030

Artisan Fume Tunnel (UDI 05700573002030)

Manufactured by Agilent Technologies Singapore (International) Pte Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Artisan Fume Tunnel - Primary ID 05700573002030

Device Regulatory Overview

The Artisan Fume Tunnel (Model/Catalog Number: AR527) is a medical device manufactured by Agilent Technologies Singapore (International) Pte Ltd. This product is indexed under FDA Product Code / Category Classification W02029099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
AR527
Product Code / EMDN
W02029099
Device Name
Artisan Fume Tunnel
Database Sync Date
2026-08-09 19:05:14

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 Artisan Fume Tunnel?

The registered manufacturer of record for Artisan Fume Tunnel is Agilent Technologies Singapore (International) Pte Ltd.

What is the Primary UDI-DI identifier for Artisan Fume Tunnel?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05700573002030.

What classification code is assigned to this device?

This device is registered under product classification code W02029099.

Programmatic Export

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

JSON API Endpoint