eudamed_udi
Primary ID: 04260702150113
preOx - HUT (UDI 04260702150113)
Manufactured by preOx.RS GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for preOx - HUT - Primary ID 04260702150113
Device Regulatory Overview
The preOx - HUT (Model/Catalog Number: 200.050) is a medical device manufactured by preOx.RS GmbH. This product is indexed under FDA Product Code / Category Classification W0105090102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 200.050
- Product Code / EMDN
- W0105090102
- Device Name
- preOx - HUT
- Database Sync Date
- 2026-08-09 16:51:14
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 preOx - HUT?
The registered manufacturer of record for preOx - HUT is preOx.RS GmbH.
What is the Primary UDI-DI identifier for preOx - HUT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260702150113.
What classification code is assigned to this device?
This device is registered under product classification code W0105090102.
Similar Classification Devices (W0105090102)
Other Devices by preOx.RS GmbH
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