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Video Laryngoscope Single Use

EUDAMED

Class I (EU MDR)

Ref FMD-005-4110-D4

by SG Manufacturers

Identity

Trade Name
Video Laryngoscope Single Use EUDAMED
Device Name
Video Laryngoscope Single Use EUDAMED
Model / Reference
FMD-005-4110-D4 EUDAMED

Identifiers

Primary DI / UDI-DI
08964004013249 EUDAMED
Basic UDI-DI
8964004013VS0274 EUDAMED
EMDN Code
Z12021004 VIDEO LARYNGOSCOPES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland 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

Video Laryngoscope Single Use by SG Manufacturers — 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
SG Manufacturers
EUDAMED SRN
PK-MF-000007106
Authorised Representative
International Business Compendious of Sweden SE-AR-000001625

Sources (1)

  • EUDAMED 9499bf96-8c01-4a66-811e-11035a193af4 61 fields · synced Oct 5, 2026