gudid
Primary ID: CELLPRESERV CYTOCENTRIFUGE
CELLPRESERV KOLPLAST (UDI CELLPRESERV CYTOCENTRIFUGE)
Manufactured by Kolplast C I
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CELLPRESERV KOLPLAST - Primary ID CELLPRESERV CYTOCENTRIFUGE
Device Regulatory Overview
The CELLPRESERV KOLPLAST (Model/Catalog Number: CELLPRESERV CYTOCENTRIFUGE) is a medical device manufactured by Kolplast C I. This product is indexed under FDA Product Code / Category Classification IFB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CELLPRESERV CYTOCENTRIFUGE
- Product Code / EMDN
- IFB
- Device Name
- Database Sync Date
- 2026-08-09 09:07:20
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 CELLPRESERV KOLPLAST?
The registered manufacturer of record for CELLPRESERV KOLPLAST is Kolplast C I.
What is the Primary UDI-DI identifier for CELLPRESERV KOLPLAST?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CELLPRESERV CYTOCENTRIFUGE.
What classification code is assigned to this device?
This device is registered under product classification code IFB.
Similar Classification Devices (IFB)
Other Devices by Kolplast C I
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