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Premature, 00

EUDAMED

Class I (EU MDR)

Ref AL-1801-00EModel AL-1801-E

by Long Life Surgical Industries

Identity

Trade Name
Premature, 00 EUDAMED
Device Name
Macintosh Single Use Eco Blade, Fiber Optic Acrylic, Semimetal EUDAMED
Model / Reference
AL-1801-E EUDAMED
AL-1801-00E EUDAMED

Identifiers

Primary DI / UDI-DI
08961102724558 EUDAMED
Basic UDI-DI
++G126SUMACFOSME54 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 1b559a4c-c76d-4005-b8a6-e21c94717381 61 fields · synced Oct 6, 2026