GUDIDData
eudamed_udi Primary ID: 06971402971547

cence (UDI 06971402971547)

Manufactured by HUNAN XIANG YI LABORATORY INSTRUMENT DEVELOPMENT CO.,LTD.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for cence - Primary ID 06971402971547

Device Regulatory Overview

The cence (Model/Catalog Number: YXL-23) is a medical device manufactured by HUNAN XIANG YI LABORATORY INSTRUMENT DEVELOPMENT CO.,LTD.. This product is indexed under FDA Product Code / Category Classification W02069003 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
YXL-23
Product Code / EMDN
W02069003
Device Name
CENTRIFUGE
Database Sync Date
2026-08-09 16:29:10

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 cence?

The registered manufacturer of record for cence is HUNAN XIANG YI LABORATORY INSTRUMENT DEVELOPMENT CO.,LTD..

What is the Primary UDI-DI identifier for cence?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06971402971547.

What classification code is assigned to this device?

This device is registered under product classification code W02069003.

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