GUDIDData
eudamed_udi Primary ID: 05700573002481

Dako CoverStainer (UDI 05700573002481)

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 Dako CoverStainer - Primary ID 05700573002481

Device Regulatory Overview

The Dako CoverStainer (Model/Catalog Number: CS100) is a medical device manufactured by Agilent Technologies Singapore (International) Pte Ltd. This product is indexed under FDA Product Code / Category Classification W0202059002 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
CS100
Product Code / EMDN
W0202059002
Device Name
Dako CoverStainer
Database Sync Date
2026-08-09 16:30:44

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 Dako CoverStainer?

The registered manufacturer of record for Dako CoverStainer is Agilent Technologies Singapore (International) Pte Ltd.

What is the Primary UDI-DI identifier for Dako CoverStainer?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05700573002481.

What classification code is assigned to this device?

This device is registered under product classification code W0202059002.

Programmatic Export

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

JSON API Endpoint