GUDIDData
eudamed_udi Primary ID: 06979488990025

BeneSupport (UDI 06979488990025)

Manufactured by CHINA BROSPER CO., LIMITED

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BeneSupport - Primary ID 06979488990025

Device Regulatory Overview

The BeneSupport (Model/Catalog Number: BeneSupport Back Support) is a medical device manufactured by CHINA BROSPER CO., LIMITED. This product is indexed under FDA Product Code / Category Classification Y061219 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
BeneSupport Back Support
Product Code / EMDN
Y061219
Device Name
Back Support
Database Sync Date
2026-08-09 17:11:53

Full Regulatory Attributes

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{
    "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 BeneSupport?

The registered manufacturer of record for BeneSupport is CHINA BROSPER CO., LIMITED.

What is the Primary UDI-DI identifier for BeneSupport?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06979488990025.

What classification code is assigned to this device?

This device is registered under product classification code Y061219.

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