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Am30bdtu

EUDAMED

Class I (EU MDR)

Ref AM30BDTU

by Brandon Medical Company Limited

Identity

Trade Name
AM30BDTU EUDAMED
Device Name
Astramax EUDAMED
Model / Reference
AM30BDTU EUDAMED

Identifiers

Primary DI / UDI-DI
05060413446562 EUDAMED
Basic UDI-DI
506041344AM30XF EUDAMED
Direct Marketing DI
05060413446562 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

Am30bdtu 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 7d1621b5-3c60-415a-8f71-e6af9494e129 61 fields · synced Jul 9, 2026