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Allegra M30

EUDAMED

Class IIa (EU MDR)

Ref 1510216HLRMModel Secretion Aspirators

by ASSKEA GmbH

Identity

Trade Name
Allegra M30 EUDAMED
Model / Reference
Secretion Aspirators EUDAMED
1510216HLRM EUDAMED

Identifiers

Primary DI / UDI-DI
04260586042160 EUDAMED
Basic UDI-DI
426058604SecretAspDN EUDAMED
Direct Marketing DI
04260586042160 EUDAMED
EMDN Code
Z12159009 EQUIPMENT FOR REMOVAL OF SECRETIONS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Ireland 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

Allegra M30 by ASSKEA GmbH — 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

Manufacturer
ASSKEA GmbH
EUDAMED SRN
DE-MF-000005146

Sources (1)

  • EUDAMED 83a3f35d-0f75-4fa9-a447-693232c9dd94 61 fields · synced Jun 19, 2026