gudid
Primary ID: 10-37001
Resistex (UDI 10-37001)
Manufactured by MERCURY ENTERPRISES, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Resistex - Primary ID 10-37001
Device Regulatory Overview
The Resistex (Model/Catalog Number: 10-37001) is a medical device manufactured by MERCURY ENTERPRISES, INC.. This product is indexed under FDA Product Code / Category Classification BWF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10-37001
- Product Code / EMDN
- BWF
- Device Name
- Database Sync Date
- 2026-08-09 09:37:15
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 Resistex?
The registered manufacturer of record for Resistex is MERCURY ENTERPRISES, INC..
What is the Primary UDI-DI identifier for Resistex?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10-37001.
What classification code is assigned to this device?
This device is registered under product classification code BWF.
Similar Classification Devices (BWF)
Other Devices by MERCURY ENTERPRISES, INC.
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