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Hermle

EUDAMED

Class I (EU MDR)

Ref 351K

by Bernhard Hermle GmbH

Identity

Trade Name
HERMLE EUDAMED
Device Name
Kanüle, Auge, lakrimal EUDAMED
Model / Reference
351K EUDAMED

Identifiers

Primary DI / UDI-DI
04260725820826 EUDAMED
Basic UDI-DI
426072582I5-KanueleLakrMC EUDAMED
Direct Marketing DI
04260725820826 EUDAMED
EMDN Code
L1713 OCULAR IRRIGATION OR SUCTION CANNULAS, 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

Category: Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable

Hermle by Bernhard Hermle GmbH — Class I — CE/MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
DE-MF-000010226

Sources (1)

  • EUDAMED b4481081-5713-4383-8b26-ac47213ed1fc 61 fields · synced Oct 7, 2026