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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

NGM WAVE Base Tray — Class I MDR by NGMedical GmbH

MD Atlas
NGMedical GmbH

EUDAMED last updated this device on Dec 19, 2025

NGM WAVE Base Tray

42516314TD021I4B

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: NGMedical GmbH
UDI-DI code: 04251631411062
Reference / catalog number: CON24

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Manufacturer information

Organization name: NGMedical GmbH
SRN: DE-MF-000000204
Manufacturer status: Active

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Critical warnings

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

CW010
EUDAMED did not publish a description for this code.
CW036
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
Ireland		Still on market

Device identification

Trade name: NGM WAVE Base Tray
UDI-DI code: 04251631411062
Basic UDI-DI: 42516314TD021I4B
Reference / catalog number: CON24
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: The container system is designed for loading NGMedical medical devices that are marketed in a non-sterile state and must be sterilised before use. Sterilisation and storage of the enclosed products is enabled and ensured until they are used.
Additional information URL: https://ngmedical.de/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V0499CLINICAL USE CONTAINERS (NON-IVD) - OTHER

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

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.