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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

013050 — Class I MDR by Helmut Schwarz GmbH

MD Atlas
Helmut Schwarz GmbH

EUDAMED last updated this device on Feb 25, 2026

013050

42511257013050DR

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Helmut Schwarz GmbH
UDI-DI code: 04251125700290
Reference / catalog number: 013050

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Manufacturer information

Organization name: Helmut Schwarz GmbH
SRN: DE-MF-000015181
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 04251125700290
Basic UDI-DI: 42511257013050DR
Reference / catalog number: 013050
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: Der melipul Mehrweg-Medikamentenbecher ist die praktische und nachhaltige Lösung für den täglichen Einsatz in Praxis, Klinik und Pflege. Mit einem Fassungsvermögen von bis zu 25 ml eignet er sich ideal für die Aufnahme von Fest- und Flüssigmedikamenten. Bei kompakten Abmessungen von 33 mm Durchmesser und 40 mm Höhe ist der Becher handlich und zugleich standsicher. Gefertigt aus grifffestem, robustem Polypropylen überzeugt er durch seine Langlebigkeit und Stabilität. Der integrierte Stapelrand ermöglicht ein sicheres Übereinanderstapeln der Becher, sodass beispielsweise unten Tabletten und darüber Flüssigkeiten vorbereitet werden können. Dadurch wird eine strukturierte und effiziente Medikamentenausgabe unterstützt. Der Becher ist stapelbar, spülmaschinengeeignet und für den Mehrwegeinsatz konzipiert.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y150915GLASSES AND CUPS

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

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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.