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Hermle

EUDAMED

Class I (EU MDR)

Ref 501

by Bernhard Hermle GmbH

Identity

Trade Name
HERMLE EUDAMED
Device Name
Schere, Auge EUDAMED
Model / Reference
501 EUDAMED

Identifiers

Primary DI / UDI-DI
04260725820154 EUDAMED
Basic UDI-DI
426072582Ir-SchereAugeV7 EUDAMED
Direct Marketing DI
04260725820154 EUDAMED
EMDN Code
L01040503 IRIS SCISSORS, 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

Hermle by Bernhard Hermle GmbH — 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

EUDAMED SRN
DE-MF-000010226

Sources (1)

  • EUDAMED dfb4102a-50fc-4918-861b-1087cef83c68 61 fields · synced Jun 18, 2026