GUDIDData
eudamed_udi Primary ID: 16944290667813

RUI (UDI 16944290667813)

Manufactured by Beijing Rongrui-Century Science & Technology Co. , Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RUI - Primary ID 16944290667813

Device Regulatory Overview

The RUI (Model/Catalog Number: RST009CA) is a medical device manufactured by Beijing Rongrui-Century Science & Technology Co. , Ltd.. This product is indexed under FDA Product Code / Category Classification C900301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
RST009CA
Product Code / EMDN
C900301
Device Name
Pulse Oximeter Sensors
Database Sync Date
2026-08-09 16:48:23

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 RUI?

The registered manufacturer of record for RUI is Beijing Rongrui-Century Science & Technology Co. , Ltd..

What is the Primary UDI-DI identifier for RUI?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 16944290667813.

What classification code is assigned to this device?

This device is registered under product classification code C900301.

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