eudamed_udi
Primary ID: 04260702150472
preOx IPS-CATH (UDI 04260702150472)
Manufactured by preOx.RS GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for preOx IPS-CATH - Primary ID 04260702150472
Device Regulatory Overview
The preOx IPS-CATH (Model/Catalog Number: 520.028) is a medical device manufactured by preOx.RS GmbH. This product is indexed under FDA Product Code / Category Classification A0699 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 520.028
- Product Code / EMDN
- A0699
- Device Name
- preOx IPS-CATH
- Database Sync Date
- 2026-08-09 18:33:39
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 IPS-CATH?
The registered manufacturer of record for preOx IPS-CATH is preOx.RS GmbH.
What is the Primary UDI-DI identifier for preOx IPS-CATH?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260702150472.
What classification code is assigned to this device?
This device is registered under product classification code A0699.
Similar Classification Devices (A0699)
Other Devices by preOx.RS GmbH
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