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Am30wjst

EUDAMED

Class I (EU MDR)

Ref AM30WJST

by Brandon Medical Company Limited

Identity

Trade Name
AM30WJST EUDAMED
Device Name
Astramax EUDAMED
Model / Reference
AM30WJST EUDAMED

Identifiers

Primary DI / UDI-DI
05060413447224 EUDAMED
Basic UDI-DI
506041344AM30XF EUDAMED
Direct Marketing DI
05060413447224 EUDAMED
EMDN Code
Z12010701 FIXED SCIALYTIC LAMPS 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

Category: Operating room light system

Am30wjst by Brandon Medical Company Limited — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Operating room light system.

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 54d26762-f54c-43cc-b2d0-711f6fcceca0 61 fields · synced Oct 6, 2026