GUDIDData
gudid Primary ID: 00020012500

HemosIL LA Positive Control (UDI 00020012500)

Manufactured by INSTRUMENTATION LABORATORY COMPANY

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HemosIL LA Positive Control - Primary ID 00020012500

Device Regulatory Overview

The HemosIL LA Positive Control (Model/Catalog Number: 00020012500) is a medical device manufactured by INSTRUMENTATION LABORATORY COMPANY. This product is indexed under FDA Product Code / Category Classification GGN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
00020012500
Product Code / EMDN
GGN
Device Name
HemosIL LA Positive Control
Database Sync Date
2026-08-09 09:10:49

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of HemosIL LA Positive Control?

The registered manufacturer of record for HemosIL LA Positive Control is INSTRUMENTATION LABORATORY COMPANY.

What is the Primary UDI-DI identifier for HemosIL LA Positive Control?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00020012500.

What classification code is assigned to this device?

This device is registered under product classification code GGN.

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