gudid
Primary ID: RK028
VERDOC (UDI RK028)
Manufactured by ALBERT BROWNE LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VERDOC - Primary ID RK028
Device Regulatory Overview
The VERDOC (Model/Catalog Number: RK028) is a medical device manufactured by ALBERT BROWNE LIMITED. This product is indexed under FDA Product Code / Category Classification JOJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RK028
- Product Code / EMDN
- JOJ
- Device Name
- The Verdoc Steam and EO Load Data Cards indicate that a load has been processed in a steam sterilization cycle.
- Database Sync Date
- 2026-08-09 10:00:19
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 VERDOC?
The registered manufacturer of record for VERDOC is ALBERT BROWNE LIMITED.
What is the Primary UDI-DI identifier for VERDOC?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RK028.
What classification code is assigned to this device?
This device is registered under product classification code JOJ.
Similar Classification Devices (JOJ)
Other Devices by ALBERT BROWNE LIMITED
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