GUDIDData
gudid Primary ID: SF-371

belter (UDI SF-371)

Manufactured by Shenzhen Belter Health Measurement and Analysis Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for belter - Primary ID SF-371

Device Regulatory Overview

The belter (Model/Catalog Number: SF-371) is a medical device manufactured by Shenzhen Belter Health Measurement and Analysis Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification MNW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SF-371
Product Code / EMDN
MNW
Device Name
Database Sync Date
2026-08-09 09:05:28

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 belter?

The registered manufacturer of record for belter is Shenzhen Belter Health Measurement and Analysis Technology Co., Ltd..

What is the Primary UDI-DI identifier for belter?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SF-371.

What classification code is assigned to this device?

This device is registered under product classification code MNW.

Similar Classification Devices (MNW)

Other Devices by Shenzhen Belter Health Measurement and Analysis Technology Co., Ltd.

Programmatic Export

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