Karaoğlu

by Karaoğlu Baskül Ve Cerrahi̇ Aletler İmal. San. Ti̇c. Ltd. Şti̇ 331 variants

Ref KB203.00Model KARAOĞLU

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	Number8699041KARAOGLU_085E Basic UDI-DI 08699041727995UDI-DI	Date14 May 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Withdrawn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

Device Name: Absorbent
Model / Reference: KARAOĞLU, KB203.00

Primary DI / UDI-DI: 08699041727995
Basic UDI-DI: 8699041KARAOGLU_085E
EMDN Code: L030101 Suction and irrigation surgical cannulas and handpieces, reusable

Device Class: Class IIa
EU market of registration: Türkiye

Manufacturer details

EUDAMED SRN: TR-MF-000041867

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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