eudamed_udi
Primary ID: 04039239017189
B.Braun (UDI 04039239017189)
Manufactured by B. Braun Avitum AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for B.Braun - Primary ID 04039239017189
Device Regulatory Overview
The B.Braun (Model/Catalog Number: 169) is a medical device manufactured by B. Braun Avitum AG. This product is indexed under FDA Product Code / Category Classification F040202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 169
- Product Code / EMDN
- F040202
- Device Name
- Alkaline HD concentrates
- Database Sync Date
- 2026-08-09 17:16:21
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 B.Braun?
The registered manufacturer of record for B.Braun is B. Braun Avitum AG.
What is the Primary UDI-DI identifier for B.Braun?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04039239017189.
What classification code is assigned to this device?
This device is registered under product classification code F040202.
Similar Classification Devices (F040202)
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