eudamed_udi
Primary ID: 03760369880213
Unspecified Brand (UDI 03760369880213)
Manufactured by AFI Centrifuge
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 03760369880213
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: AFI-C200RH/IVD) is a medical device manufactured by AFI Centrifuge. This product is indexed under FDA Product Code / Category Classification W02069005 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AFI-C200RH/IVD
- Product Code / EMDN
- W02069005
- Device Name
- LISA reversible centrifuge, 120V IVD
- Database Sync Date
- 2026-08-09 17:20:37
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is AFI Centrifuge.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03760369880213.
What classification code is assigned to this device?
This device is registered under product classification code W02069005.
Similar Classification Devices (W02069005)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint