gudid
Primary ID: Series 2 PRO PLUS C/US
Celluma (UDI Series 2 PRO PLUS C/US)
Manufactured by Biophotas, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Celluma - Primary ID Series 2 PRO PLUS C/US
Device Regulatory Overview
The Celluma (Model/Catalog Number: Series 2 PRO PLUS C/US) is a medical device manufactured by Biophotas, Inc.. This product is indexed under FDA Product Code / Category Classification OLP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Series 2 PRO PLUS C/US
- Product Code / EMDN
- OLP
- Device Name
- 4 mode large panel light therapy device
- Database Sync Date
- 2026-08-09 09:49:38
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 Celluma?
The registered manufacturer of record for Celluma is Biophotas, Inc..
What is the Primary UDI-DI identifier for Celluma?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Series 2 PRO PLUS C/US.
What classification code is assigned to this device?
This device is registered under product classification code OLP.
Similar Classification Devices (OLP)
Other Devices by Biophotas, Inc.
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