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Extrémité remaplacement P/19070

EUDAMED

Class I (EU MDR)

Ref 19076Model 19009

by Moria S.A.

Identity

Trade Name
Extrémité remaplacement P/19070 EUDAMED
Device Name
Beehler Pupil Dilator. straight EUDAMED
Model / Reference
19009 EUDAMED
19076 EUDAMED

Identifiers

Primary DI / UDI-DI
03700483605644 EUDAMED
Basic UDI-DI
37004836Iris-Retractors5U EUDAMED
EMDN Code
L170102 OCULAR AND ENDOCULAR RETRACTORS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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

Extrémité remaplacement P/19070 by Moria S.A. — 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
Moria S.A.
EUDAMED SRN
FR-MF-000000336

Sources (1)

  • EUDAMED 4060f60f-1c49-49aa-83ed-5f4889c5419f 61 fields · synced Jun 18, 2026