gudid
Primary ID: PCC005
VERIFY (UDI PCC005)
Manufactured by ALBERT BROWNE LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VERIFY - Primary ID PCC005
Device Regulatory Overview
The VERIFY (Model/Catalog Number: PCC005) 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
- PCC005
- Product Code / EMDN
- JOJ
- Device Name
- The VERIFY SixCess 250F 30 Minute Indicator Short are cycle verification indicators which are designed to react to all critical variables for specific sterilization cycles.
- 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 VERIFY?
The registered manufacturer of record for VERIFY is ALBERT BROWNE LIMITED.
What is the Primary UDI-DI identifier for VERIFY?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PCC005.
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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