gudid
Primary ID: EZ Single Cytofunnel Brown
Epredia (UDI EZ Single Cytofunnel Brown)
Manufactured by SHANDON DIAGNOSTICS LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Epredia - Primary ID EZ Single Cytofunnel Brown
Device Regulatory Overview
The Epredia (Model/Catalog Number: EZ Single Cytofunnel Brown) is a medical device manufactured by SHANDON DIAGNOSTICS LIMITED. This product is indexed under FDA Product Code / Category Classification IFB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EZ Single Cytofunnel Brown
- Product Code / EMDN
- IFB
- Device Name
- Cytospin 4 Cytocentrifuge - Accessory
- Database Sync Date
- 2026-08-09 09:39:59
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 Epredia?
The registered manufacturer of record for Epredia is SHANDON DIAGNOSTICS LIMITED.
What is the Primary UDI-DI identifier for Epredia?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is EZ Single Cytofunnel Brown.
What classification code is assigned to this device?
This device is registered under product classification code IFB.
Similar Classification Devices (IFB)
Other Devices by SHANDON DIAGNOSTICS LIMITED
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