Laryngoscope Blade, Reusable

by SG Manufacturers 210 variants

Ref FMG-001-2394-01

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number8964003248MR228K Basic UDI-DI 08964004001116UDI-DI	Date16 Mar 2026Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference: FMG-001-2394-01

Primary DI / UDI-DI: 08964004001116
Basic UDI-DI: 8964003248MR228K
EMDN Code: Z12021003 Laryngoscopes

Device Class: Class I
EU market of registration: Poland

Manufacturer details

EUDAMED SRN: PK-MF-000007106
Authorised representative: International Business Compendious of Sweden SE-AR-000001625

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Properties

Reusable

Other properties (12)

Sterile: No
Implantable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No