eudamed_udi
Primary ID: 04046955876105
AQUAboss® (UDI 04046955876105)
Manufactured by B. Braun Avitum AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AQUAboss® - Primary ID 04046955876105
Device Regulatory Overview
The AQUAboss® (Model/Catalog Number: LA1170151) is a medical device manufactured by B. Braun Avitum AG. This product is indexed under FDA Product Code / Category Classification Z12099007 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LA1170151
- Product Code / EMDN
- Z12099007
- Device Name
- Aquaboss nX
- Database Sync Date
- 2026-08-09 16:47:33
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 AQUAboss®?
The registered manufacturer of record for AQUAboss® is B. Braun Avitum AG.
What is the Primary UDI-DI identifier for AQUAboss®?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04046955876105.
What classification code is assigned to this device?
This device is registered under product classification code Z12099007.
Similar Classification Devices (Z12099007)
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