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Laryngoscope Blade, Reusable

EUDAMED

Class I (EU MDR)

Ref FMC-003-3020-04

by Haymed Instruments

Identity

Trade Name
Laryngoscope Blade, Reusable EUDAMED
Device Name
Laryngoscope Blade, Reusable EUDAMED
Model / Reference
FMC-003-3020-04 EUDAMED

Identifiers

Primary DI / UDI-DI
08964003352431 EUDAMED
Basic UDI-DI
8964003352HM015B EUDAMED
EMDN Code
Z12021003 LARYNGOSCOPES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland 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

Laryngoscope Blade, Reusable by Haymed Instruments — 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

Manufacturer
Haymed Instruments
EUDAMED SRN
PK-MF-000012992
Authorised Representative
International Business Compendious of Sweden SE-AR-000001625

Sources (1)

  • EUDAMED e9bdd806-bf55-4459-b389-24438162ddef 61 fields · synced Jun 19, 2026