GUDIDData
eudamed_udi Primary ID: 06945936702113

BEE III 400 (UDI 06945936702113)

Manufactured by Xiamen NewSound Technology Co.,Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BEE III 400 - Primary ID 06945936702113

Device Regulatory Overview

The BEE III 400 (Model/Catalog Number: 06945936702113) is a medical device manufactured by Xiamen NewSound Technology Co.,Ltd. This product is indexed under FDA Product Code / Category Classification Y2145060201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
06945936702113
Product Code / EMDN
Y2145060201
Device Name
hearing aids
Database Sync Date
2026-08-09 16:29:06

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of BEE III 400?

The registered manufacturer of record for BEE III 400 is Xiamen NewSound Technology Co.,Ltd.

What is the Primary UDI-DI identifier for BEE III 400?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06945936702113.

What classification code is assigned to this device?

This device is registered under product classification code Y2145060201.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint