Organization name

B. Braun Avitum AG

SRN

DE-MF-000005127

Manufacturer status

Active

1 warning recorded — scroll inside the panel to see all entries.

• Refer to instruction manual/booklet

Primary placement in Germany; available across 27 countries total.

Trade name

AQUAboss®

UDI-DI code

Primary DI

The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.

04046955875559

Basic UDI-DI

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

403923900000192839

Reference / catalog number

LA1140400

Issuing entity

UDI issuing entities

Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.

GS1

Risk category

MDR risk classes

MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.

Class IIb

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

AQUAboss nX I 4000 400V 50/60Hz

Additional information URL

https://eifu.bbraun.com/

Clinical sizes

No clinical sizes registered for this device.

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

European Medical Device Nomenclature — the EU product classification assigned to this device.

• Z12099007DIALYSIS WATER TREATMENT SYSTEMS

• Class IIb medical devices in EUDAMED

Certificate health across this manufacturer's portfolio.

No certificate specifically references this device's Basic UDI-DI.