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Ocular and endocular retractors, reusable

EUDAMED

Class I (EU MDR)

Ref L170102

by Clinimed

Identity

Trade Name
Ocular and endocular retractors, reusable EUDAMED
Device Name
Ocular and endocular retractors, reusable EUDAMED
Model / Reference
L170102 EUDAMED

Identifiers

Primary DI / UDI-DI
M294L1701020 EUDAMED
Basic UDI-DI
++M294L170102E5 EUDAMED
EMDN Code
L170102 OCULAR AND ENDOCULAR RETRACTORS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Ocular and endocular retractors, reusable by Clinimed — 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
Clinimed
EUDAMED SRN
US-MF-000033329
Authorised Representative
ANTEX MEDI SOLUTION DE-AR-000008078

Sources (1)

  • EUDAMED 2f38997c-4985-4ec6-a56a-539efc8ff0b1 61 fields · synced Jun 18, 2026