gudid
Primary ID: PCC079
Celerity (UDI PCC079)
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 PCC079
Device Regulatory Overview
The Celerity (Model/Catalog Number: PCC079) is a medical device manufactured by ALBERT BROWNE LIMITED. This product is indexed under FDA Product Code / Category Classification QKM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PCC079
- Product Code / EMDN
- QKM
- Device Name
- Celerity HP Multivariable CI is designed for routine monitoring of Lumen, Non-Lumen, Flexible, Fast Non Lumen, Fast sterilization cycle of a V-PRO Low Temperature Sterilization System, or Standard, Advanced, Express, Flex Scope or Duo cycles of an ASP STERRAD System, including those systems with ALLClear Technology.
- 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 PCC079.
What classification code is assigned to this device?
This device is registered under product classification code QKM.
Similar Classification Devices (QKM)
Other Devices by ALBERT BROWNE LIMITED
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