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Laryngoscope, Otoscope and Accessories

EUDAMED

Class I (EU MDR)

Ref AV.1356.02

by Gimmi GmbH

Identity

Device Name
Laryngoscope, Otoscope and Accessories EUDAMED
Model / Reference
AV.1356.02 EUDAMED

Identifiers

Primary DI / UDI-DI
04049047027065 EUDAMED
Basic UDI-DI
4049047ZAJ03AFA27DROVX EUDAMED
Direct Marketing DI
04049047027065 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

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

Category: Laryngoscope blade, reusable

Laryngoscope, Otoscope and Accessories by Gimmi Gmbh — 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

Manufacturer
Gimmi GmbH
EUDAMED SRN
DE-MF-000005445

Sources (1)

  • EUDAMED 7f025253-7463-4f97-9c2a-9eb9997d38d6 61 fields · synced Jun 19, 2026