GUDIDData
gudid Primary ID: 06260060100

GEM Check Coag Control-Abnormal for APTT (UDI 06260060100)

Manufactured by INSTRUMENTATION LABORATORY COMPANY

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GEM Check Coag Control-Abnormal for APTT - Primary ID 06260060100

Device Regulatory Overview

The GEM Check Coag Control-Abnormal for APTT (Model/Catalog Number: 06260060100) 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
06260060100
Product Code / EMDN
GGN
Device Name
GEM Check Coag Control-Abnormal for APTT
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 GEM Check Coag Control-Abnormal for APTT?

The registered manufacturer of record for GEM Check Coag Control-Abnormal for APTT is INSTRUMENTATION LABORATORY COMPANY.

What is the Primary UDI-DI identifier for GEM Check Coag Control-Abnormal for APTT?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06260060100.

What classification code is assigned to this device?

This device is registered under product classification code GGN.

Programmatic Export

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

JSON API Endpoint