GUDIDData
gudid Primary ID: 00020002400

HemosIL Wash-R Emulsion (UDI 00020002400)

Manufactured by INSTRUMENTATION LABORATORY COMPANY

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HemosIL Wash-R Emulsion - Primary ID 00020002400

Device Regulatory Overview

The HemosIL Wash-R Emulsion (Model/Catalog Number: 00020002400) is a medical device manufactured by INSTRUMENTATION LABORATORY COMPANY. This product is indexed under FDA Product Code / Category Classification JPA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
00020002400
Product Code / EMDN
JPA
Device Name
HemosIL Wash-R Emulsion 1000 mL
Database Sync Date
2026-08-09 09:10:50

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 HemosIL Wash-R Emulsion?

The registered manufacturer of record for HemosIL Wash-R Emulsion is INSTRUMENTATION LABORATORY COMPANY.

What is the Primary UDI-DI identifier for HemosIL Wash-R Emulsion?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00020002400.

What classification code is assigned to this device?

This device is registered under product classification code JPA.

Programmatic Export

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

JSON API Endpoint