gudid
Primary ID: CD129
CO2 (UDI CD129)
Manufactured by RANDOX LABORATORIES LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CO2 - Primary ID CD129
Device Regulatory Overview
The CO2 (Model/Catalog Number: CD129) is a medical device manufactured by RANDOX LABORATORIES LIMITED. This product is indexed under FDA Product Code / Category Classification KHS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CD129
- Product Code / EMDN
- KHS
- Device Name
- The device is intended for the quantitative in vitro determination of carbon dioxide in serum or plasma.
- Database Sync Date
- 2026-08-09 09:39:53
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 CO2?
The registered manufacturer of record for CO2 is RANDOX LABORATORIES LIMITED.
What is the Primary UDI-DI identifier for CO2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CD129.
What classification code is assigned to this device?
This device is registered under product classification code KHS.
Similar Classification Devices (KHS)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint