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ERGOJECT 2.0-BL Injector

EUDAMED

Class IIa (EU MDR)

Ref ERB2000Model IOL injectors

by Medicel AG

Identity

Trade Name
ERGOJECT 2.0-BL Injector EUDAMED
Device Name
IOL injectors EUDAMED
Model / Reference
IOL injectors EUDAMED
ERB2000 EUDAMED

Identifiers

Primary DI / UDI-DI
07630055213570 EUDAMED
Basic UDI-DI
076300552INJ01YD EUDAMED
Direct Marketing DI
07630055213570 EUDAMED
EMDN Code
Q021111 OCULAR IMPLANT INSTRUMENTS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

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

ERGOJECT 2.0-BL Injector by Medicel AG — Class IIa — 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
Medicel AG
EUDAMED SRN
CH-MF-000016652
Authorised Representative
Rudolf Riester GmbH DE-AR-000015844

Sources (1)

  • EUDAMED e83124a9-a0f1-4d78-93ca-e5351bdbca61 61 fields · synced Jun 18, 2026