eudamed_udi
Primary ID: 03760369880091
AFI (UDI 03760369880091)
Manufactured by AFI Centrifuge
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AFI - Primary ID 03760369880091
Device Regulatory Overview
The AFI (Model/Catalog Number: AFI-CI060V/IVD) is a medical device manufactured by AFI Centrifuge. This product is indexed under FDA Product Code / Category Classification W02069003 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AFI-CI060V/IVD
- Product Code / EMDN
- W02069003
- Device Name
- ISA Ventilated Centrifuge, 120V 60Hz
- Database Sync Date
- 2026-08-09 16:51:59
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 AFI?
The registered manufacturer of record for AFI is AFI Centrifuge.
What is the Primary UDI-DI identifier for AFI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03760369880091.
What classification code is assigned to this device?
This device is registered under product classification code W02069003.
Similar Classification Devices (W02069003)
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