eudamed_udi
Primary ID: 04260702150069
preOx LOR (UDI 04260702150069)
Manufactured by preOx.RS GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for preOx LOR - Primary ID 04260702150069
Device Regulatory Overview
The preOx LOR (Model/Catalog Number: 100.032) is a medical device manufactured by preOx.RS GmbH. This product is indexed under FDA Product Code / Category Classification A020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 100.032
- Product Code / EMDN
- A020101
- Device Name
- preOx LOR
- Database Sync Date
- 2026-08-09 18:39:43
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 LOR?
The registered manufacturer of record for preOx LOR is preOx.RS GmbH.
What is the Primary UDI-DI identifier for preOx LOR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260702150069.
What classification code is assigned to this device?
This device is registered under product classification code A020101.
Similar Classification Devices (A020101)
Other Devices by preOx.RS GmbH
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