eudamed_udi
Primary ID: 04547410467703
FDR CROSS (UDI 04547410467703)
Manufactured by FUJIFILM Corporation
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FDR CROSS - Primary ID 04547410467703
Device Regulatory Overview
The FDR CROSS (Model/Catalog Number: 04547410467703) is a medical device manufactured by FUJIFILM Corporation. This product is indexed under FDA Product Code / Category Classification Z11039017 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 04547410467703
- Product Code / EMDN
- Z11039017
- Device Name
- DR-XD 3000
- Database Sync Date
- 2026-08-09 16:28:57
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 FDR CROSS?
The registered manufacturer of record for FDR CROSS is FUJIFILM Corporation.
What is the Primary UDI-DI identifier for FDR CROSS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04547410467703.
What classification code is assigned to this device?
This device is registered under product classification code Z11039017.
Similar Classification Devices (Z11039017)
Other Devices by FUJIFILM Corporation
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