Ceylan

by Fatma Ceylan- Ceylan Medi̇kal İmalat İthalat İhracat Diş Ti̇caret 867 variants

Ref CKB-K-115Model CEYLAN

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number86810926CEYLAN13730K4 Basic UDI-DI 08681092606671UDI-DI	Date6 Apr 2024Registered	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Withdrawn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: Sterilization Container Systems
Model / Reference: CEYLAN, CKB-K-115

Primary DI / UDI-DI: 08681092606671
Basic UDI-DI: 86810926CEYLAN13730K4
EMDN Code: S010401 Trays, baskets, tubs for sterilisation and their components

Device Class: Class I
EU market of registration: Türkiye

Manufacturer details

EUDAMED SRN: TR-MF-000039137

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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