gudid
Primary ID: ETG-4000
Hitachi (UDI ETG-4000)
Manufactured by HITACHI, LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Hitachi - Primary ID ETG-4000
Device Regulatory Overview
The Hitachi (Model/Catalog Number: ETG-4000) is a medical device manufactured by HITACHI, LTD.. This product is indexed under FDA Product Code / Category Classification DQA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ETG-4000
- Product Code / EMDN
- DQA
- Device Name
- 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 Hitachi?
The registered manufacturer of record for Hitachi is HITACHI, LTD..
What is the Primary UDI-DI identifier for Hitachi?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ETG-4000.
What classification code is assigned to this device?
This device is registered under product classification code DQA.
Similar Classification Devices (DQA)
Other Devices by HITACHI, LTD.
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