GUDIDData
eudamed_udi Primary ID: 06974600260482

BonSensor (UDI 06974600260482)

Manufactured by Changzhou Boen Zhongding Medical Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BonSensor - Primary ID 06974600260482

Device Regulatory Overview

The BonSensor (Model/Catalog Number: DR2) is a medical device manufactured by Changzhou Boen Zhongding Medical Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z11030402 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
DR2
Product Code / EMDN
Z11030402
Device Name
Digital ntraoral X-Ray Imaging System
Database Sync Date
2026-08-09 16:46:06

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 BonSensor?

The registered manufacturer of record for BonSensor is Changzhou Boen Zhongding Medical Technology Co., Ltd..

What is the Primary UDI-DI identifier for BonSensor?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974600260482.

What classification code is assigned to this device?

This device is registered under product classification code Z11030402.

Similar Classification Devices (Z11030402)

Other Devices by Changzhou Boen Zhongding Medical Technology Co., Ltd.

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