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X-Large-5

EUDAMED

Class I (EU MDR)

Ref AL-1803-5EModel AL-1803-E

by Long Life Surgical Industries

Identity

Trade Name
X-Large-5 EUDAMED
Device Name
Macintosh Single Use Blade Fiber Optic, Acrylic, Metallic EUDAMED
Model / Reference
AL-1803-E EUDAMED
AL-1803-5E EUDAMED

Identifiers

Primary DI / UDI-DI
08964002476770 EUDAMED
Basic UDI-DI
++G126SUMACFOFME33 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

X-Large-5 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 de8b56ca-1c6a-45bc-8bb2-b5328e93e4b6 61 fields · synced Jun 18, 2026