gudid
Primary ID: MG5801
Amethyst (UDI MG5801)
Manufactured by Medgluv Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Amethyst - Primary ID MG5801
Device Regulatory Overview
The Amethyst (Model/Catalog Number: MG5801) is a medical device manufactured by Medgluv Inc.. This product is indexed under FDA Product Code / Category Classification QDO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MG5801
- Product Code / EMDN
- QDO
- Device Name
- Amethyst Nitrile Exam Gloves, Reflex Blue, Small
- Database Sync Date
- 2026-08-09 09:37:49
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 Amethyst?
The registered manufacturer of record for Amethyst is Medgluv Inc..
What is the Primary UDI-DI identifier for Amethyst?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MG5801.
What classification code is assigned to this device?
This device is registered under product classification code QDO.
Similar Classification Devices (QDO)
Other Devices by Medgluv Inc.
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