eudamed_udi
Primary ID: 06974842441106
CELUTION (UDI 06974842441106)
Manufactured by Cytori Therapeutics LLC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CELUTION - Primary ID 06974842441106
Device Regulatory Overview
The CELUTION (Model/Catalog Number: Celution 805) is a medical device manufactured by Cytori Therapeutics LLC.. This product is indexed under FDA Product Code / Category Classification A0399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Celution 805
- Product Code / EMDN
- A0399
- Device Name
- Celution 805 Consumable Set
- Database Sync Date
- 2026-08-09 18:41:42
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 CELUTION?
The registered manufacturer of record for CELUTION is Cytori Therapeutics LLC..
What is the Primary UDI-DI identifier for CELUTION?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974842441106.
What classification code is assigned to this device?
This device is registered under product classification code A0399.
Similar Classification Devices (A0399)
Other Devices by Cytori Therapeutics LLC.
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