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Injector

EUDAMED

Class I (EU MDR)

Ref M-2908Model InjectorRef M-257Ref M-2808Ref M-256

by CILITA Ltd.

Identity

Device Name
Injector EUDAMED
Model / Reference
Injector EUDAMED
M-2908 EUDAMED
M-257 EUDAMED
M-2808 EUDAMED
M-256 EUDAMED

Identifiers

Primary DI / UDI-DI
04610274509749 EUDAMED
04610274509671 EUDAMED
04610274509718 EUDAMED
04610274509664 EUDAMED
Basic UDI-DI
468017344CILINJBH EUDAMED
EMDN Code
L1709 OCULAR IMPLANT INSTRUMENTS NOT INCLUDED IN OTHER CLASSES, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Portugal EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Injector by CILITA Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
CILITA Ltd.
EUDAMED SRN
RU-MF-000041168
Authorised Representative
Arazy Group GmbH DE-AR-000007685

Sources (4)

  • EUDAMED e318aa23-73af-4a41-a873-173b9fa287cd 61 fields · synced Sep 17, 2026
  • EUDAMED 77d0c0ef-de7d-45e1-9f1e-9be7ded3c3a3 61 fields · synced May 18, 2026
  • EUDAMED bfe19bbd-0a60-460b-a7e1-52c790452d5c 61 fields · synced May 18, 2026
  • EUDAMED 4fa0b98c-f6f8-488c-b2df-159364f66fee 61 fields · synced May 19, 2026