Uamed

by UAMED Surgical Industries 101 variants

Ref Sl-105-01

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDR

Ended

Withdrawn

Date not published (CE MDR)

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

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	Number++G215SI10501EQ Basic UDI-DI ++G215SI10501UDI-DI	Date19 Sep 2024Registered	StatusWithdrawn No longer placed on the EU market

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Withdrawn

Specification

EUDAMED

Device Name: Flexible Tip Fiber Optic Laryngoscope Blade Size 1
Model / Reference: Sl-105-01

Primary DI / UDI-DI: ++G215SI10501
Basic UDI-DI: ++G215SI10501EQ
Direct Marketing DI: ++G215SI10501
EMDN Code: Z12021003 Laryngoscopes

Device Class: Class I
EU market of registration: Germany

Manufacturer details

EUDAMED SRN: PK-MF-000029358
Authorised representative: Yellow's medical instruments GmbH DE-AR-000007390

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Class I
Uamed

Class I
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Properties

Other properties (13)

Sterile: No
Implantable: No
Reusable: 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