gudid
Primary ID: 9099-30
Tronex International, Inc. (UDI 9099-30)
Manufactured by TRONEX INTERNATIONAL, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Tronex International, Inc. - Primary ID 9099-30
Device Regulatory Overview
The Tronex International, Inc. (Model/Catalog Number: 9099-30) is a medical device manufactured by TRONEX INTERNATIONAL, INC.. This product is indexed under FDA Product Code / Category Classification QDO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9099-30
- Product Code / EMDN
- QDO
- Device Name
- Glove, Exam, Nitrile, Chemotherapy Rated, Fingertip-Textured, 12", Powder-Free, Latex-Free, Blue, Large
- Database Sync Date
- 2026-08-09 09:38:20
Full Regulatory Attributes
🔒 Token Gated
{
"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 Tronex International, Inc.?
The registered manufacturer of record for Tronex International, Inc. is TRONEX INTERNATIONAL, INC..
What is the Primary UDI-DI identifier for Tronex International, Inc.?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9099-30.
What classification code is assigned to this device?
This device is registered under product classification code QDO.
Similar Classification Devices (QDO)
Other Devices by TRONEX INTERNATIONAL, INC.
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