Unspecified Brand (UDI 00678467002921)
Manufactured by Mui Scientific, Division of H&A Mui Enterprises Inc.
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: SPR1B(150)) is a medical device manufactured by Mui Scientific, Division of H&A Mui Enterprises Inc.. This product is indexed under FDA Product Code / Category Classification G020301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SPR1B(150)
- Product Code / EMDN
- G020301
- Device Name
- PVC Single Use Catheter
- Database Sync Date
- 2026-08-09 17:04:43
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Mui Scientific, Division of H&A Mui Enterprises Inc..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00678467002921.
What classification code is assigned to this device?
This device is registered under product classification code G020301.
Similar Classification Devices (G020301)
Other Devices by Mui Scientific, Division of H&A Mui Enterprises Inc.
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