gudid
Primary ID: UST-9127
UST-9127 (UDI UST-9127)
Manufactured by FUJIFILM CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for UST-9127 - Primary ID UST-9127
Device Regulatory Overview
The UST-9127 (Model/Catalog Number: UST-9127) 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
- UST-9127
- Product Code / EMDN
- IYO
- Device Name
- Probe
- Database Sync Date
- 2026-08-09 09:15:37
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 UST-9127?
The registered manufacturer of record for UST-9127 is FUJIFILM CORPORATION.
What is the Primary UDI-DI identifier for UST-9127?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is UST-9127.
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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint