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Durotip®

EUDAMED

Class I (EU MDR)

Ref BC231R

by Aesculap AG

Identity

Trade Name
DUROTIP® EUDAMED
Device Name
Ring scissors Ir EUDAMED
Model / Reference
BC231R EUDAMED

Identifiers

Primary DI / UDI-DI
04038653137688 EUDAMED
Basic UDI-DI
403923900000062023 EUDAMED
Direct Marketing DI
04038653137688 EUDAMED
EMDN Code
L010403 SURGICAL DISSECTION 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

Yes

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: General-purpose surgical scissors, reusable

Durotip® by Aesculap AG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose surgical scissors, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Aesculap AG
EUDAMED SRN
DE-MF-000005504

Sources (1)

  • EUDAMED 9b269bf2-26b3-4770-ba85-8bcb0f98e248 61 fields · synced Jun 20, 2026