eudamed_udi
Primary ID: 05056408923521
Transactive Xtra (UDI 05056408923521)
Manufactured by Prism Medical UK
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Transactive Xtra - Primary ID 05056408923521
Device Regulatory Overview
The Transactive Xtra (Model/Catalog Number: 1001TX134220Â ) is a medical device manufactured by Prism Medical UK. This product is indexed under FDA Product Code / Category Classification V08050302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1001TX134220Â
- Product Code / EMDN
- V08050302
- Device Name
- Freeway Transactive Xtra 130 - MTÂ
- Database Sync Date
- 2026-08-09 16:48:18
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 Transactive Xtra?
The registered manufacturer of record for Transactive Xtra is Prism Medical UK.
What is the Primary UDI-DI identifier for Transactive Xtra?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05056408923521.
What classification code is assigned to this device?
This device is registered under product classification code V08050302.
Similar Classification Devices (V08050302)
Other Devices by Prism Medical UK
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