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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

01043 — Class I MDR by Helmut Schwarz GmbH

MD Atlas
Helmut Schwarz GmbH

EUDAMED last updated this device on Feb 25, 2026

01043

42511257010401DB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Helmut Schwarz GmbH
UDI-DI code: 04251125700177
Reference / catalog number: 01043

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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: 04251125700177
Basic UDI-DI: 42511257010401DB
Reference / catalog number: 01043
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: 10
Additional product description: Der melinip Schnabelbecher apart Deckel ist die passgenaue Ergänzung zum 250-ml-Becherunterteil und unterstützt eine sichere sowie komfortable Anwendung im Alltag. Gefertigt aus hochwertigem Kunststoff überzeugt der Deckel, als Trink oder Breideckel, durch seine stabile Ausführung und zuverlässige Passform. Er ist mikrowellengeeignet und spülmaschinengeeignet bis 93 °C und damit für den hygienischen Mehrfacheinsatz geeignet. Der Deckel ist als eigenständiges Produkt mit separater UDI-DI geführt und ideal für den Einsatz in Pflege, Klinik und häuslicher Versorgung.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y150999ASSISTIVE EATING AND DRINKING DEVICES - 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

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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.