gudid
Primary ID: LCC028
VERIFY (UDI LCC028)
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 LCC028
Device Regulatory Overview
The VERIFY (Model/Catalog Number: LCC028) is a medical device manufactured by ALBERT BROWNE LIMITED. This product is indexed under FDA Product Code / Category Classification FLG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LCC028
- Product Code / EMDN
- FLG
- Device Name
- VERIFY DualAction Ultrasonic Indicator Holder is used with the VERIFY DualAction Ultrasonic Indicator.
- Database Sync Date
- 2026-08-09 09:19:08
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 LCC028.
What classification code is assigned to this device?
This device is registered under product classification code FLG.
Similar Classification Devices (FLG)
Other Devices by ALBERT BROWNE LIMITED
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