JBC (UDI 400-1048)

Manufactured by FOREMOUNT ENTERPRISE CO., LTD.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The JBC (Model/Catalog Number: 400-1048) is a medical device manufactured by FOREMOUNT ENTERPRISE CO., LTD.. This product is indexed under FDA Product Code / Category Classification BYD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 400-1048
Product Code / EMDN: BYD
Device Name: Tracheal HME
Database Sync Date: 2026-08-09 09:15:28

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 JBC?

The registered manufacturer of record for JBC is FOREMOUNT ENTERPRISE CO., LTD..

What is the Primary UDI-DI identifier for JBC?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 400-1048.

What classification code is assigned to this device?

This device is registered under product classification code BYD.

Similar Classification Devices (BYD)

Other Devices by FOREMOUNT ENTERPRISE CO., LTD.

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