gudid
Primary ID: SPR1R(150)
Mui Scientific (UDI SPR1R(150))
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 SPR1R(150)
Device Regulatory Overview
The Mui Scientific (Model/Catalog Number: SPR1R(150)) 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
- SPR1R(150)
- Product Code / EMDN
- FFX
- Device Name
- Catheter Single-Use Anorectal Expulsion
- 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 SPR1R(150).
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
Programmatic Export
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JSON API Endpoint