gudid
Primary ID: F37
F37 (UDI F37)
Manufactured by FUJIFILM CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for F37 - Primary ID F37
Device Regulatory Overview
The F37 (Model/Catalog Number: F37) is a medical device manufactured by FUJIFILM CORPORATION. This product is indexed under FDA Product Code / Category Classification IYO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- F37
- Product Code / EMDN
- IYO
- Device Name
- Diagnostic Ultrasound System
- Database Sync Date
- 2026-08-09 09:15:37
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 F37?
The registered manufacturer of record for F37 is FUJIFILM CORPORATION.
What is the Primary UDI-DI identifier for F37?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is F37.
What classification code is assigned to this device?
This device is registered under product classification code IYO.
Similar Classification Devices (IYO)
Other Devices by FUJIFILM CORPORATION
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