GUDIDData
gudid Primary ID: 6129CS

MARK3 (UDI 6129CS)

Manufactured by CARGUS INTERNATIONAL, INC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MARK3 - Primary ID 6129CS

Device Regulatory Overview

The MARK3 (Model/Catalog Number: 6129CS) is a medical device manufactured by CARGUS INTERNATIONAL, INC. This product is indexed under FDA Product Code / Category Classification JOJ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
6129CS
Product Code / EMDN
JOJ
Device Name
Sterilization Indicator Tape 1" 60 Yards 40/cs. - MARK3
Database Sync Date
2026-08-09 09:05:50

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 MARK3?

The registered manufacturer of record for MARK3 is CARGUS INTERNATIONAL, INC.

What is the Primary UDI-DI identifier for MARK3?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6129CS.

What classification code is assigned to this device?

This device is registered under product classification code JOJ.

Programmatic Export

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

JSON API Endpoint