gudid
Primary ID: 2D93Q0
Revital-Ox (UDI 2D93Q0)
Manufactured by STERIS CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Revital-Ox - Primary ID 2D93Q0
Device Regulatory Overview
The Revital-Ox (Model/Catalog Number: 2D93Q0) is a medical device manufactured by STERIS CORPORATION. This product is indexed under FDA Product Code / Category Classification PHT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2D93Q0
- Product Code / EMDN
- PHT
- Device Name
- Revital-Ox Rigid Container System is for the transport or soaking of rigid endoscopes and accessories.
- Database Sync Date
- 2026-08-09 09:19:10
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 Revital-Ox?
The registered manufacturer of record for Revital-Ox is STERIS CORPORATION.
What is the Primary UDI-DI identifier for Revital-Ox?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2D93Q0.
What classification code is assigned to this device?
This device is registered under product classification code PHT.
Similar Classification Devices (PHT)
Other Devices by STERIS CORPORATION
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