GUDIDData
gudid Primary ID: FM-200

Doppler Fetal Heart Rate Detector (UDI FM-200)

Manufactured by Shenzhen Biocare Bio-Medical Equipment Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Doppler Fetal Heart Rate Detector - Primary ID FM-200

Device Regulatory Overview

The Doppler Fetal Heart Rate Detector (Model/Catalog Number: FM-200) is a medical device manufactured by Shenzhen Biocare Bio-Medical Equipment Co., Ltd.. This product is indexed under FDA Product Code / Category Classification KNG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
FM-200
Product Code / EMDN
KNG
Device Name
Database Sync Date
2026-08-09 09:04:56

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 Doppler Fetal Heart Rate Detector?

The registered manufacturer of record for Doppler Fetal Heart Rate Detector is Shenzhen Biocare Bio-Medical Equipment Co., Ltd..

What is the Primary UDI-DI identifier for Doppler Fetal Heart Rate Detector?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FM-200.

What classification code is assigned to this device?

This device is registered under product classification code KNG.

Programmatic Export

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

JSON API Endpoint