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Premature, 00

EUDAMED

Class I (EU MDR)

Ref AL-1209-00Model AL-1209

by Long Life Surgical Industries

Identity

Trade Name
Premature, 00 EUDAMED
Device Name
Wis-Hipple Reusable Blade American Profile, Conventional System EUDAMED
Model / Reference
AL-1209 EUDAMED
AL-1209-00 EUDAMED

Identifiers

Primary DI / UDI-DI
08964002478750 EUDAMED
Basic UDI-DI
++G126RUSPCONWISHAPGN EUDAMED
Direct Marketing DI
08964002478750 EUDAMED
EMDN Code
Z12021003 LARYNGOSCOPES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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: Laryngoscope blade, reusable

Premature, 00 by Long Life Surgical Industries — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Laryngoscope blade, reusable.

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 9076724f-8dfe-4211-9741-d19631bcedf2 61 fields · synced Jun 19, 2026