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Premature, 00

EUDAMED

Class I (EU MDR)

Ref AL-1804-00Model AL-1804

by Long Life Surgical Industries

Identity

Trade Name
Premature, 00 EUDAMED
Device Name
Miller Single Use Blade Fiber Optic Acrylic, Metallic EUDAMED
Model / Reference
AL-1804 EUDAMED
AL-1804-00 EUDAMED

Identifiers

Primary DI / UDI-DI
08964002476541 EUDAMED
Basic UDI-DI
++G126SUMILFOFMTB EUDAMED
EMDN Code
R9002 LARYNGOSCOPE BLADES, SINGLE-USE EUDAMED

Classification

Device Class
Class I 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

Premature, 00 by Long Life Surgical Industries — 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
PK-MF-000010701
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED 9c8dfc23-42e9-430e-86ed-6e3b1ee59301 61 fields · synced Jun 19, 2026