VERISURE (UDI 73191)
Manufactured by TERRAGENE S.A.
Device Regulatory Overview
The VERISURE (Model/Catalog Number: 73191) is a medical device manufactured by TERRAGENE S.A.. This product is indexed under FDA Product Code / Category Classification JOJ within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- 73191
- Product Code / EMDN
- JOJ
- Device Name
- VERISURE Bowie-Dick Test Card
- Database Sync Date
- 2026-08-09 09:07:22
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 VERISURE?
The registered manufacturer of record for VERISURE is TERRAGENE S.A..
What is the Primary UDI-DI identifier for VERISURE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 73191.
What classification code is assigned to this device?
This device is registered under product classification code JOJ.
Similar Classification Devices (JOJ)
Other Devices by TERRAGENE S.A.
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