Agremon

by Özden Tip Tibbi̇ Ci̇haz Ve Malzemeler Gida Teksti̇l Ti̇c.ltd.şti̇. 138 variants

Ref İNFRARUJ-AMPULModel AGREMON

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	Number868407652AGREMON_07KU Basic UDI-DI 08684076520741UDI-DI	Date15 Sep 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Withdrawn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: Reusable Instruments
Model / Reference: AGREMON, İNFRARUJ-AMPUL

Primary DI / UDI-DI: 08684076520741
Basic UDI-DI: 868407652AGREMON_07KU
EMDN Code: Z12010785 Scialytic lamp lighting systems - consumables

Device Class: Class I
EU market of registration: Türkiye

Manufacturer details

EUDAMED SRN: TR-MF-000046965

Other devices from Özden Tip Tibbi̇ Ci̇haz Ve Malzemeler Gida Teksti̇l Ti̇c.ltd.şti̇.

Agremon

Class I
Agremon

Class I
Agremon

Class I
Agremon

Class I
Agremon

Class I
Agremon

Class I

See all devices from Özden Tip Tibbi̇ Ci̇haz Ve Malzemeler Gida Teksti̇l Ti̇c.ltd.şti̇. →

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