GUDIDData
gudid Primary ID: 115-050572-00

IBP_CO_SidestreamCO2 module(FDA/FJ)II (UDI 115-050572-00)

Manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IBP_CO_SidestreamCO2 module(FDA/FJ)II - Primary ID 115-050572-00

Device Regulatory Overview

The IBP_CO_SidestreamCO2 module(FDA/FJ)II (Model/Catalog Number: 115-050572-00) is a medical device manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. This product is indexed under FDA Product Code / Category Classification CCJ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
115-050572-00
Product Code / EMDN
CCJ
Device Name
Database Sync Date
2026-08-09 09:11:05

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 IBP_CO_SidestreamCO2 module(FDA/FJ)II?

The registered manufacturer of record for IBP_CO_SidestreamCO2 module(FDA/FJ)II is Shenzhen Mindray Bio-Medical Electronics Co., Ltd..

What is the Primary UDI-DI identifier for IBP_CO_SidestreamCO2 module(FDA/FJ)II?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 115-050572-00.

What classification code is assigned to this device?

This device is registered under product classification code CCJ.

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