GUDIDData
eudamed_udi Primary ID: 04046955239214

DiaStream® (UDI 04046955239214)

Manufactured by B. Braun Avitum AG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DiaStream® - Primary ID 04046955239214

Device Regulatory Overview

The DiaStream® (Model/Catalog Number: 7211349) is a medical device manufactured by B. Braun Avitum AG. This product is indexed under FDA Product Code / Category Classification F020101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
7211349
Product Code / EMDN
F020101
Device Name
DiaStream
Database Sync Date
2026-08-09 16:30:24

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of DiaStream®?

The registered manufacturer of record for DiaStream® is B. Braun Avitum AG.

What is the Primary UDI-DI identifier for DiaStream®?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04046955239214.

What classification code is assigned to this device?

This device is registered under product classification code F020101.

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