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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Aquaboss nX — 90 UDI-DI variants, MDR (B. Braun Avitum AG)

MD Atlas
B. Braun Avitum AG

Data from EUDAMED, last updated May 23, 2026

Aquaboss nX

403923900000192839

90 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: B. Braun Avitum AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 403923900000192839
Device name: Aquaboss nX
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Sep 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: B. Braun Avitum AG
SRN: DE-MF-000005127
Country: Germany
Email: eudamed@bbraun.com
Phone: +49 5661 710

Variants by status

UDI-DI variants

90 UDI-DI variants

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Applied filters

basicUdiUlid01K5C05YDYBV6E8AC2MNHMPY76

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

AQUAboss®04046955876013
AQUAboss®04046955875092
AQUAboss®04046955875504
AQUAboss®04046955876242
AQUAboss®04046955876105
AQUAboss®04046955875672
AQUAboss®04046955875924
AQUAboss®04046955876037
AQUAboss®04046955876136
AQUAboss®04046955876006
AQUAboss®04046955876068
AQUAboss®04046955875832
AQUAboss®04046955875979
AQUAboss®04046955875580
AQUAboss®04046955875573

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