gudid
Primary ID: Series 2 LITE C/US
Celluma (UDI Series 2 LITE 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 LITE C/US
Device Regulatory Overview
The Celluma (Model/Catalog Number: Series 2 LITE 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 LITE C/US
- Product Code / EMDN
- OLP
- Device Name
- 4 mode small panel light therapy device
- Database Sync Date
- 2026-08-09 09:49:38
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 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 LITE 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.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint