gudid
Primary ID: LCC016
VERIFY (UDI LCC016)
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 LCC016
Device Regulatory Overview
The VERIFY (Model/Catalog Number: LCC016) 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
- LCC016
- Product Code / EMDN
- JOJ
- Device Name
- Chemical Indicator for SYSTEM 1E Processor
- Database Sync Date
- 2026-08-09 10:00:19
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
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 LCC016.
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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint