McIntosh Laryngoscope with 3 Curved Blades

by Mehrish Industries Pvt Ltd

Ref M01-037-00

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number++G410M0103700QF Basic UDI-DI G410M01037000UDI-DI	Date8 Jun 2023Registered	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Withdrawn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: M01-037-00

Primary DI / UDI-DI: G410M01037000
Basic UDI-DI: ++G410M0103700QF
EMDN Code: Z12021003 Laryngoscopes

Device Class: Class I
EU market of registration: Romania

Manufacturer details

EUDAMED SRN: PK-MF-000031501
Authorised representative: ANTEX MEDI SOLUTION DE-AR-000008078

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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