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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

5999880412100 — Class IIa MDR by Illés Csók és Társa…

MD Atlas
Illés Csók és Társa Vegyeskereskedő Korlátolt Felelősségű Társaság

EUDAMED last updated this device on May 12, 2026

5999880412100

5999880412AriannaCP

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Illés Csók és Társa Vegyeskereskedő Korlátolt Felelősségű Társaság
UDI-DI code: 05999880412100
Reference / catalog number: 5999880412100

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Manufacturer information

Organization name: Illés Csók és Társa Vegyeskereskedő Korlátolt Felelősségű Társaság
SRN: HU-MF-000004639
Manufacturer status: Active

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.

Market distribution

Primary placement in Hungary; available across 1 country total.

Country	On market since	Until
HungaryPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 05999880412100
Basic UDI-DI: 5999880412AriannaCP
Reference / catalog number: 5999880412100
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

R05010399MUCOSITY ASPIRATORS - 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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