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Lar. 080.70.1660a

EUDAMED

Class I (EU MDR)

Ref 9AJI-1012Ref 9AJI-1013

by Blazejewski MEDI-TECH GmbH

Identity

Device Name
Lar. 080.70.1660a EUDAMED
Model / Reference
9AJI-1012 EUDAMED
9AJI-1013 EUDAMED

Identifiers

Primary DI / UDI-DI
D-9AJI-1012H9 EUDAMED
D-9AJI-1013HB EUDAMED
Basic UDI-DI
B-9AJI-1012H9 EUDAMED
B-9AJI-1013HB 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Lar. 080.70.1660a by Blazejewski MEDI-TECH GmbH — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
DE-MF-000005467

Sources (2)

  • EUDAMED aece3c21-4646-46ff-b2e8-051e1f91107b 61 fields · synced Jul 15, 2026
  • EUDAMED 8a52702f-fc99-446f-8e81-9368201f1483 61 fields · synced May 18, 2026