eudamed_udi
Primary ID: 04260702150090
preOx IAP (UDI 04260702150090)
Manufactured by preOx.RS GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for preOx IAP - Primary ID 04260702150090
Device Regulatory Overview
The preOx IAP (Model/Catalog Number: 100.071) is a medical device manufactured by preOx.RS GmbH. This product is indexed under FDA Product Code / Category Classification A070199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 100.071
- Product Code / EMDN
- A070199
- Device Name
- preOx - IAP Adapter-Set
- Database Sync Date
- 2026-08-09 16:47:03
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 IAP?
The registered manufacturer of record for preOx IAP is preOx.RS GmbH.
What is the Primary UDI-DI identifier for preOx IAP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260702150090.
What classification code is assigned to this device?
This device is registered under product classification code A070199.
Similar Classification Devices (A070199)
Other Devices by preOx.RS GmbH
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