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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

10000 — Class I MDR by Elysium Laboratories Kft.

MD Atlas
Elysium Laboratories Kft.

EUDAMED last updated this device on Jul 16, 2025

10000

5999862705CMB01M3

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Elysium Laboratories Kft.
UDI-DI code: 05999862705152
Reference / catalog number: 10000

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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
Gyermekektől távol tartandó! Szembe, szájba, sebbe nem kerülhet! 12 éven aluli gyermek esetében kizárólag felnőtt használhatja! Bőrirritáció esetén ne használja tovább, hanem forduljon azonnal szakorvoshoz!

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: 05999862705152
Basic UDI-DI: 5999862705CMB01M3
Reference / catalog number: 10000
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)

V901001LICE ELIMINATION MECHANICAL DEVICES

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

Related devices

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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.