GUDIDData
gudid Primary ID: FD-590G

My Baby's Heartbeat Bear Fetal Doppler (UDI FD-590G)

Manufactured by Vcomin Technlogy Limited

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for My Baby's Heartbeat Bear Fetal Doppler - Primary ID FD-590G

Device Regulatory Overview

The My Baby's Heartbeat Bear Fetal Doppler (Model/Catalog Number: FD-590G) is a medical device manufactured by Vcomin Technlogy Limited. This product is indexed under FDA Product Code / Category Classification KNG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
FD-590G
Product Code / EMDN
KNG
Device Name
Database Sync Date
2026-08-09 09:06:47

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 My Baby's Heartbeat Bear Fetal Doppler?

The registered manufacturer of record for My Baby's Heartbeat Bear Fetal Doppler is Vcomin Technlogy Limited.

What is the Primary UDI-DI identifier for My Baby's Heartbeat Bear Fetal Doppler?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FD-590G.

What classification code is assigned to this device?

This device is registered under product classification code KNG.

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