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Organization name
UDI-DI code
Reference / catalog number

4-2223-02-04 — Class I MDD by STELLA Kunststofftechnik…

MD Atlas
STELLA Kunststofftechnik GmbH

EUDAMED last updated this device on Apr 30, 2026

4-2223-02-04

B-04262385230007

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: STELLA Kunststofftechnik GmbH
UDI-DI code: 04262385230007
Reference / catalog number: 4-2223-02-04

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Manufacturer information

Organization name: STELLA Kunststofftechnik GmbH
SRN: DE-MF-000007777
Manufacturer status: Active

Related devices

4-2233-00-34B-04262385230021On the market 4-4433-00-05B-04262385230106On the market 4-4435-00-05B-04262385230113On the market 4-4443-00-34B-04262385230168On the market 4-4436-03-74B-04262385230250On the market

Market distribution

Primary placement in Germany; available across 3 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
Italy		Still on market
Netherlands		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04262385230007
Basic UDI-DI: B-04262385230007
Reference / catalog number: 4-2223-02-04
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: This is a non-sterile cup for dosage and application of liquid preparations for oral use (Praeparationes liquidae peroraliae). The cup is intended to be marketed as component of the finished medicinal product attached to the finished medicinal product. At any rate, the suitability of this here described measuring cup for a particular content is to be tested fully and on the own responsibility by the user.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V0399MEASUREMENT 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

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.