gudid
Primary ID: HT110
Transonic (UDI HT110)
Manufactured by TRANSONIC SYSTEMS INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Transonic - Primary ID HT110
Device Regulatory Overview
The Transonic (Model/Catalog Number: HT110) is a medical device manufactured by TRANSONIC SYSTEMS INC.. This product is indexed under FDA Product Code / Category Classification DPW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HT110
- Product Code / EMDN
- DPW
- Device Name
- Database Sync Date
- 2026-08-09 09:26:42
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 Transonic?
The registered manufacturer of record for Transonic is TRANSONIC SYSTEMS INC..
What is the Primary UDI-DI identifier for Transonic?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HT110.
What classification code is assigned to this device?
This device is registered under product classification code DPW.
Similar Classification Devices (DPW)
Other Devices by TRANSONIC SYSTEMS INC.
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