eudamed_udi
Primary ID: 00840733102318
Revogene® (UDI 00840733102318)
Manufactured by Meridian Bioscience Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Revogene® - Primary ID 00840733102318
Device Regulatory Overview
The Revogene® (Model/Catalog Number: 610210) is a medical device manufactured by Meridian Bioscience Inc.. This product is indexed under FDA Product Code / Category Classification W02050116 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 610210
- Product Code / EMDN
- W02050116
- Device Name
- Revogene®
- Database Sync Date
- 2026-08-09 16:47:10
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 Revogene®?
The registered manufacturer of record for Revogene® is Meridian Bioscience Inc..
What is the Primary UDI-DI identifier for Revogene®?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840733102318.
What classification code is assigned to this device?
This device is registered under product classification code W02050116.
Similar Classification Devices (W02050116)
Other Devices by Meridian Bioscience Inc.
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