gudid
Primary ID: R2000CC
Firehouse (UDI R2000CC)
Manufactured by FOREMOUNT ENTERPRISE CO., LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Firehouse - Primary ID R2000CC
Device Regulatory Overview
The Firehouse (Model/Catalog Number: R2000CC) is a medical device manufactured by FOREMOUNT ENTERPRISE CO., LTD.. This product is indexed under FDA Product Code / Category Classification CBP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- R2000CC
- Product Code / EMDN
- CBP
- Device Name
- White Hard Case Adult/Child
- 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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Firehouse?
The registered manufacturer of record for Firehouse is FOREMOUNT ENTERPRISE CO., LTD..
What is the Primary UDI-DI identifier for Firehouse?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is R2000CC.
What classification code is assigned to this device?
This device is registered under product classification code CBP.
Similar Classification Devices (CBP)
Other Devices by FOREMOUNT ENTERPRISE CO., LTD.
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