eudamed_udi
Primary ID: 06974842442103
Celbrush (UDI 06974842442103)
Manufactured by Cytori Therapeutics LLC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Celbrush - Primary ID 06974842442103
Device Regulatory Overview
The Celbrush (Model/Catalog Number: 503/CRS) is a medical device manufactured by Cytori Therapeutics LLC.. This product is indexed under FDA Product Code / Category Classification A0280 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 503/CRS
- Product Code / EMDN
- A0280
- Device Name
- Celbrush
- Database Sync Date
- 2026-08-09 16:50:44
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 Celbrush?
The registered manufacturer of record for Celbrush is Cytori Therapeutics LLC..
What is the Primary UDI-DI identifier for Celbrush?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974842442103.
What classification code is assigned to this device?
This device is registered under product classification code A0280.
Similar Classification Devices (A0280)
Other Devices by Cytori Therapeutics LLC.
Programmatic Export
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