gudid
Primary ID: C7-R1-1003
Mui Scientific (UDI C7-R1-1003)
Manufactured by H & A Mui Enterprises Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Mui Scientific - Primary ID C7-R1-1003
Device Regulatory Overview
The Mui Scientific (Model/Catalog Number: C7-R1-1003) is a medical device manufactured by H & A Mui Enterprises Inc. This product is indexed under FDA Product Code / Category Classification FFX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C7-R1-1003
- Product Code / EMDN
- FFX
- Device Name
- 1-Channel Customized Anorectal Catheter with Balloon
- Database Sync Date
- 2026-08-09 09:00:34
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 Mui Scientific?
The registered manufacturer of record for Mui Scientific is H & A Mui Enterprises Inc.
What is the Primary UDI-DI identifier for Mui Scientific?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is C7-R1-1003.
What classification code is assigned to this device?
This device is registered under product classification code FFX.
Similar Classification Devices (FFX)
Other Devices by H & A Mui Enterprises Inc
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