eudamed_udi
Primary ID: 04046955904792
OMNI® (UDI 04046955904792)
Manufactured by B. Braun Avitum AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OMNI® - Primary ID 04046955904792
Device Regulatory Overview
The OMNI® (Model/Catalog Number: 7107516) is a medical device manufactured by B. Braun Avitum AG. This product is indexed under FDA Product Code / Category Classification Z12090201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7107516
- Product Code / EMDN
- Z12090201
- Device Name
- OMNI
- Database Sync Date
- 2026-08-09 16:29:57
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 OMNI®?
The registered manufacturer of record for OMNI® is B. Braun Avitum AG.
What is the Primary UDI-DI identifier for OMNI®?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04046955904792.
What classification code is assigned to this device?
This device is registered under product classification code Z12090201.
Similar Classification Devices (Z12090201)
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