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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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Organization name
UDI-DI code
Reference / catalog number

4180 — Class IIa MDD by NOUVAG AG

MD Atlas
NOUVAG AG

EUDAMED last updated this device on May 20, 2026

4180

B-+ENOU41800G

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: NOUVAG AG
UDI-DI code: +ENOU41800G
Reference / catalog number: 4180

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Manufacturer information

Organization name: NOUVAG AG
SRN: CH-MF-000018882
Manufacturer status: Active

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW010
The Dispenser DP 30 may only be operated under constant supervision of medical personnel. The absence of a warning buzz to indicate malfunctions of the device requires the permanent control of the volumetric displacement of the pump.
CW007
Do not use the device if the shipping box has holes/cracks on the flat surfaces, and/or if the Styrofoam protective packaging is broken.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jan 1, 2013	Still on market

Device identification

Trade name: not provided
UDI-DI code: +ENOU41800G
Basic UDI-DI: B-+ENOU41800G
Reference / catalog number: 4180
Issuing entity: HIBCC

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Infusion pump, general-purpose.
Additional information URL: https://www.nouvag.com/
Clinical sizes: 60–230 MU57
Maximal Pressure — 2.5 MU126

EMDN nomenclature code(s)

Z12030301INFUSION PUMPS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.