GUDIDData
gudid Primary ID: 3x2ml

Daniel (UDI 3x2ml)

Manufactured by Jiangxi Dentalbright Technology Co., Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Daniel - Primary ID 3x2ml

Device Regulatory Overview

The Daniel (Model/Catalog Number: 3x2ml) is a medical device manufactured by Jiangxi Dentalbright Technology Co., Ltd. This product is indexed under FDA Product Code / Category Classification MAU within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
3x2ml
Product Code / EMDN
MAU
Device Name
Database Sync Date
2026-08-09 09:05:22

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 Daniel?

The registered manufacturer of record for Daniel is Jiangxi Dentalbright Technology Co., Ltd.

What is the Primary UDI-DI identifier for Daniel?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3x2ml.

What classification code is assigned to this device?

This device is registered under product classification code MAU.

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