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Hermle

EUDAMED

Class I (EU MDR)

Ref 2001

by Bernhard Hermle GmbH

Identity

Trade Name
HERMLE EUDAMED
Device Name
Trephine, Korneal EUDAMED
Model / Reference
2001 EUDAMED

Identifiers

Primary DI / UDI-DI
04260725822417 EUDAMED
Basic UDI-DI
426072582Ir-TrephinKorSF9 EUDAMED
Direct Marketing DI
04260725822417 EUDAMED
EMDN Code
L170401 CORNEAL TREPHINES, 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: Corneoscleral punch

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

Similar devices

Also classified as Corneoscleral punch.

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 ae961855-cebc-415f-907a-0af0c9adeb1f 61 fields · synced Jun 19, 2026