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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

10023 — Class I MDR by Elysium Laboratories Kft.

MD Atlas
Elysium Laboratories Kft.

EUDAMED last updated this device on Jul 17, 2025

10023

5999862705TCK01S5

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Elysium Laboratories Kft.
UDI-DI code: 05999862705435
Reference / catalog number: 10023

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Manufacturer information

Organization name: Elysium Laboratories Kft.
SRN: HU-MF-000039543
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW011
• Csak orvosi célokra használható! Az eszközt kizárólag kullancsok eltávolítására használja. • Ne próbálja meg kézzel eltávolítani a kullancsot. • A készletben található csipeszek hegyesek. Ne használja őket arra, hogy önmagában, vagy másokban kárt tegyen. • Ne használjon körömlakkot, alkoholt, petrolátumot vagy hőt a kullancs eltávolítására. • Ne fertőtlenítse az eszközöket mérgező vagy maró vegyszerekkel. • Ha nem biztos benne hogyan kell a kullancsot eltávolítani, kérjen segítséget szakembertől. • A kullancsok által terjesztett betegségek (pl. Lyme-kór, agyvelőgyulladás, TIBOLA stb.) súlyosak lehetnek, ezért fontos, hogy figyelje a kullancs eltávolítása utáni tüneteket, és amennyiben szükséges, forduljon orvoshoz. • Gyermekektől elzárva tárolandó.

Market distribution

Primary placement in Hungary; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 05999862705435
Basic UDI-DI: 5999862705TCK01S5
Reference / catalog number: 10023
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z120499GENERAL MEDICINE INSTRUMENTS - 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.