gudid
Primary ID: LCC015
Celerity (UDI LCC015)
Manufactured by ALBERT BROWNE LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Celerity - Primary ID LCC015
Device Regulatory Overview
The Celerity (Model/Catalog Number: LCC015) 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
- LCC015
- Product Code / EMDN
- JOJ
- Device Name
- Celerity Chemical Indicator for enspire 3000 CLCSPS employing S40 Sterilant.
- 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 Celerity?
The registered manufacturer of record for Celerity is ALBERT BROWNE LIMITED.
What is the Primary UDI-DI identifier for Celerity?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is LCC015.
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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