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MEIKO TopLine 30

EUDAMED

Class IIa (EU MDR)

Ref -

by MEIKO Maschinenbau GmbH & Co. KG

Identity

Trade Name
MEIKO TopLine 30 EUDAMED
Device Name
MEIKO TopLine EUDAMED
Model / Reference
- EUDAMED

Identifiers

Primary DI / UDI-DI
04050187000108 EUDAMED
Basic UDI-DI
4050187001ZV EUDAMED
Direct Marketing DI
04050187000108 EUDAMED
EMDN Code
Z12011301 CLEANING AND DISINFECTION EQUIPMENT EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

MEIKO TopLine 30 by MEIKO Maschinenbau GmbH & Co. KG — Class IIa — 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
DE-MF-000005536

Sources (1)

  • EUDAMED 3872a439-3902-47c8-b7db-0c8e26a562cc 61 fields · synced Jun 19, 2026