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14605

EUDAMED

Class I (EU MDR)

Ref 14605

by Brandon Medical Company Limited

Identity

Trade Name
14605 EUDAMED
Device Name
Astralite EUDAMED
Model / Reference
14605 EUDAMED

Identifiers

Primary DI / UDI-DI
05060413445862 EUDAMED
Basic UDI-DI
506041344AL10X4 EUDAMED
Direct Marketing DI
05060413445862 EUDAMED
EMDN Code
Z12010799 SCIALYTIC LAMP LIGHTING SYSTEMS - OTHER EUDAMED

Classification

Device Class
Class I 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

14605 by Brandon Medical Company Limited — 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
GB-MF-000005501
Authorised Representative
RegTrac Limited IE-AR-000042448

Sources (1)

  • EUDAMED 39365e95-c144-4705-addc-afb33183a52d 61 fields · synced Oct 6, 2026