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HESS! Fém tetűfésű nagyítóval PP foglalatban

EUDAMED

Class I (EU MDR)

Ref 10001

by Elysium Laboratories Kft.

Identity

Trade Name
HESS! Fém tetűfésű nagyítóval PP foglalatban EUDAMED
Device Name
Tetűfésű EUDAMED
Model / Reference
10001 EUDAMED

Identifiers

Primary DI / UDI-DI
05999862705169 EUDAMED
Basic UDI-DI
5999862705CMB01M3 EUDAMED
EMDN Code
V901001 LICE ELIMINATION MECHANICAL DEVICES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Hungary EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

HESS! Fém tetűfésű nagyítóval PP foglalatban by Elysium Laboratories Kft. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
HU-MF-000039543

Sources (1)

  • EUDAMED b3f24414-ab7d-4242-ab85-9118342cb640 61 fields · synced Jun 19, 2026